What’s New for 2015
- C-Level Panel: Cutting Edge Insights on China’s Growing Biotech Market
- China FDA Special Address
- 80+ Key Expert Speakers from Asia’s leading Pharma & Biotech
- 1 Joint Exhibition & Networking Area
- 4 Days of Expert Knowledge Sharing
- Revamped Program with New Special Focused Tracks & Sessions
Biologics World Taiwan 2016 (email me at justin.dejesus@imapac.com) Justin Barin de Jesus
The ONLY biopharmaceutical
gathering in Taiwan
Emphasizes on new business collaborations, demonstrate state-of-the-art developments and to propel Taiwan's biotech firms onto the world stage.
Cell Line Development and Engineering 2015 Rita Barry
The 4th Annual Cell Line Development & Engineering Asia conference is a must attend event for you to get the latest updates and best practices in Cell Line Generation, Bioprocessing and Antibodies Development!
This exclusive forum is where industry experts will share lessons learned through case studies, strategic discussion groups and interactive roundtables to collectively collaborate and provide solutions to your most pressing challenges. Bring back new ideas to do better business!
4 Reasons Why You Must Attend this 2015
1. Update yourself with latest technologies to accelerate every stage of cell line development with maximum efficiency, quality and reduced cost
2. Enhance cell line generation in the early stages with best practices in transfection, optimizing cell culture media, and implement advancements in clone screening and selection techniques
3. Gain effective bioprocess control & optimization strategies, for efficient, safe and cost effective scale-up
4. Latest cutting edge updates on antibody development- novel screening strategies for target discovery, challenges in ADCs, engineering bispecifics and boosting efficacy in antibody therapeutics
http://www.celllineasia.com
Pharmaceutical Congress China 29-30 March 2016Helen P
Bringing 3 Significant Events Under 1 Roof!
The Pharmaceutical Congress China, part of IBC’s PharmaCon Series, recognizes the importance of regulation, clinical operation efficiencies, tackling pharmaceutical compliance issues and bringing products and services successfully in the market in China’s rapidly advancing pharmaceutical industry.
What's new this Year?
NEW LOCATION - Hong Kong.
PLASMA FRACTIONATION TECHNOLOGY WORKSHOP.
REGULATOR’S FORUM - meet Global and Asian regulatory experts for plasma and blood products.
GLOBAL EMERGING MARKETS Self Sufficiency Case Studies: China, India, Iran and more.
INSIGHTS to the first South East Asian plasma fractionation plant.
No other Bioplasma event can get you one-to-one access to senior decision-makers from both the international and regional Bioplasma industry.
Quality for Biologics ' New ReportCritical quality attributes, process and change control, product variation, characterisation, and regulatory concernsSales of biologics grew by 20% in 2007, far faster than sales of small molecule drugs, which grew by not much more than 5%. The number of biologics being launched is also growing very rapidly, accounting for more than 25% of launches in 2007. But biologics are not like small molecules ' they are more complex to develop, test and produce. Any change in production may have a direct effect on both safety and efficacy. Making sure that development, testing and production is done correctly can be expensive, but getting it wrong can be even more expensive and may be disastrous for patients and for the companies involved.This unique 300 page report can help you to understand the processes involved ' knowledge that can save time and money and even make the difference between success and failure. The report covers all aspects of the subject including' Critical quality attributes ' Manufacturing process parameters' Process analytical technology' Physicochemical analysis,' Bioassays, ' Formulation and specifications' Product- and process-related impurities' Aggregation ' Non-clinical testing' Clinical development, ' Post-marketing period' Regulatory authority expectations' Risk management ' Comparability concernsQuality for Biologics is edited by Dr Nicole Lyscom and is written by senior industry experts from leading companies and organisations including:UCBUCB-CelltechEli LillyAmgenRocheParexel ConsultingGenentech
Biologics World Taiwan 2016 (email me at justin.dejesus@imapac.com) Justin Barin de Jesus
The ONLY biopharmaceutical
gathering in Taiwan
Emphasizes on new business collaborations, demonstrate state-of-the-art developments and to propel Taiwan's biotech firms onto the world stage.
Cell Line Development and Engineering 2015 Rita Barry
The 4th Annual Cell Line Development & Engineering Asia conference is a must attend event for you to get the latest updates and best practices in Cell Line Generation, Bioprocessing and Antibodies Development!
This exclusive forum is where industry experts will share lessons learned through case studies, strategic discussion groups and interactive roundtables to collectively collaborate and provide solutions to your most pressing challenges. Bring back new ideas to do better business!
4 Reasons Why You Must Attend this 2015
1. Update yourself with latest technologies to accelerate every stage of cell line development with maximum efficiency, quality and reduced cost
2. Enhance cell line generation in the early stages with best practices in transfection, optimizing cell culture media, and implement advancements in clone screening and selection techniques
3. Gain effective bioprocess control & optimization strategies, for efficient, safe and cost effective scale-up
4. Latest cutting edge updates on antibody development- novel screening strategies for target discovery, challenges in ADCs, engineering bispecifics and boosting efficacy in antibody therapeutics
http://www.celllineasia.com
Pharmaceutical Congress China 29-30 March 2016Helen P
Bringing 3 Significant Events Under 1 Roof!
The Pharmaceutical Congress China, part of IBC’s PharmaCon Series, recognizes the importance of regulation, clinical operation efficiencies, tackling pharmaceutical compliance issues and bringing products and services successfully in the market in China’s rapidly advancing pharmaceutical industry.
What's new this Year?
NEW LOCATION - Hong Kong.
PLASMA FRACTIONATION TECHNOLOGY WORKSHOP.
REGULATOR’S FORUM - meet Global and Asian regulatory experts for plasma and blood products.
GLOBAL EMERGING MARKETS Self Sufficiency Case Studies: China, India, Iran and more.
INSIGHTS to the first South East Asian plasma fractionation plant.
No other Bioplasma event can get you one-to-one access to senior decision-makers from both the international and regional Bioplasma industry.
Quality for Biologics ' New ReportCritical quality attributes, process and change control, product variation, characterisation, and regulatory concernsSales of biologics grew by 20% in 2007, far faster than sales of small molecule drugs, which grew by not much more than 5%. The number of biologics being launched is also growing very rapidly, accounting for more than 25% of launches in 2007. But biologics are not like small molecules ' they are more complex to develop, test and produce. Any change in production may have a direct effect on both safety and efficacy. Making sure that development, testing and production is done correctly can be expensive, but getting it wrong can be even more expensive and may be disastrous for patients and for the companies involved.This unique 300 page report can help you to understand the processes involved ' knowledge that can save time and money and even make the difference between success and failure. The report covers all aspects of the subject including' Critical quality attributes ' Manufacturing process parameters' Process analytical technology' Physicochemical analysis,' Bioassays, ' Formulation and specifications' Product- and process-related impurities' Aggregation ' Non-clinical testing' Clinical development, ' Post-marketing period' Regulatory authority expectations' Risk management ' Comparability concernsQuality for Biologics is edited by Dr Nicole Lyscom and is written by senior industry experts from leading companies and organisations including:UCBUCB-CelltechEli LillyAmgenRocheParexel ConsultingGenentech
Why you should attend:
1. Learn from in-depth case studies on strategic partnering and effective collaboration
2. Explore new business opportunities and strategies to reach the biosimilars market in the region
3. Gain insights into the regulatory landscape for biosimilars in China, India, Korea, Taiwan and more
4. Gather the latest market intelligence and analysis and identify new trends and opportunities in Biosimilars R&D, contract manufacturing and commercialization in Asia
报名参加的五大理由
1. 深入学习有关与亚洲公司建立战略合作和有效协作的案例研究
2. 探索新的商机和战略,以便进入当地的生物仿制药市场
3. 深入了解中国、印度、韩国、台湾以及更多国家或地区的生物仿制药监管形势
4. 收集最新的市场情报和分析,确定生物仿制药研发、合同制造和商业化在亚洲的新趋势和机会
Hear about:
Biopharma Regulatory Updates and Development
Victoria Elegant, VP Medical & Regulatory Affairs, Baxter, China
Andrea Laslop, Head of Scientific Office, Austrian Agency for Food and Health Safety, Austrian Member, European Medicines Agency
Arvind Mishra, Global Head of Quality & Regulatory & Head of Strategic Business Unit, Biologicals, Cadilla Pharmaceutical, India
Advances in Biosimilars R&D
Jeffrey Su, CSO, Cytovance Biologics, USA
Wenzhi Tian, CEO, Huabo Biopharma, China
Ming Wang, President and COO, Gan & Lee Pharmaceuticals, China
Feng Li, CEO, Beijing Mabworks, China
Shaligram Rane, Vice President for Quality, Intas Pharmaceuticals, India
Understanding Obstacles and Hurdles for Entering the Biosimilars Market
Khai Meng Ang, Vice President Asia, Hospira, China
Jason Li, Senior Director, Genor Biopharma, China
Sachidananda Moorthy, Vice President - Clinical Research, Medical and Regulatory Affairs, Avesthagen, India
Sameer Agarwal, Senior Vice President, Business Center Strategic Marketing, Business Unit Generic Drugs & Standard Solutions, Fresenius Kabi, Germany
What can Asia Learn from Global Biosimilars Development and Litigation?
Li Cai, Regional R&D Counsel, Pfizer, China
Vivek Mittal, Head – Legal, Lupin, India
Viren Mahurkar, Managing Director, HitechnRock Advisors, Singapore
http://www.biosimilarsasia.com
Pre-Conference Special Focus Day, 20 May 2014
Clinical Development for Biosimilars
Post-Conference Workshops, 23 May 2014
A: Challenges in Demonstrating Biosimilarity and Interchangeability of Biosimilar Products
B: Successfully Bringing Biosimilars to Market
会前特别关注日,2014 年 5 月 20 日
生物仿制药的临床开发
会后研讨会,2014 年 5 月 23 日
A:在展示生物仿制药产品的生物相似性和可互换性方面所面临的挑战
B:成功地将生物仿制药推向市场
What’s NEW in 2015’s program?
• More case studies on successful commercialization
• Insights on developing biosimilars under new CFDA guideline
• Emerging business models in regulated and developing markets
• New and timely topics on:
o Valuating biosimilars investments
o Successful technology transfer
o Key criteria in gaining approval
Also, NEW Expert Faculty includes:
Dr Shin Jae Chang, Vice President, Celltrion, Korea
Ira Jacobs, Global Oncology Lead, Biosimilars, Pfizer, US
Paul Thomas, Business Unit Head – Biosimilars, Biocon, India
Dr. Martina A. Sersch, Global Clinical Lead, Oncology Global Development, APAC Biotherapeutics Lead, Genentech, Inc. / F. Hoffmann-La Roche Ltd.
Raj Kannan, Vice President, Commercial Head, Biosimilars, Merck, Switzerland
Huiguo (Forrest) Hu, General Manager of International Business, Shanghai CP Guojian Pharmaceutical Co., Ltd, China
Ko Chung Lin, Chief Executive Officer, PharmaEssentia Corporation, Taiwan
Wen Yong, Vice Director, Drug Research Institutes, Biopharmaceutical Institute, Jiangsu AoSaiKang Pharmaceutical Co Ltd, China
http://www.biosimilarsasia.com
“A key source of growth in biologics over the next several years will be Biomanufacturing” Ge Li, Chairman and CEO, Wuxi” <outsourcing-pharma.com,>
“Other issues with single-use include standardization of systems, the dependability to vendors, and the supply chain and waste management but if we can overcome extractables and leachables, we will eventually be able to scale up to many thousands of liters.” Jason Li, Senior Director, Downstream Processing, Genor Biopharma <biopharma-reporter.com,>
Industry experts will discuss these and more at the 5th Annual Biomanufacturing Conference in Grand Hyatt Shanghai, China on 19 – 22 May 2015 during IBC’s Biopharma Development & Production (BDP) Week.
Biomanufacturing in China: Technologies and Facility DesignRita Barry
Join us as we DISCOVER, ANALYZE and LEARN the current state of the global biomanufacturing industry and the future growth potential and recent developments in Asia.
Some of the Key Highlights You Won’t Want to Miss Include
USA
Smart & Flexible Manufacturing Solutions in Multi-Product Facilities
Franz Walz, Executive Director Global Manufacturing, Science and Technology & Network Coordination, BOEHRINGER INGELHEIM
EUROPE
MAb Manufacturing Facilities for China & Automated Single-Use Processing to Bring Control & Flexibility to Manufacturing
Pauline Nicholson, Global Product Manager, Allegro Single-Use Systems, PALL
Niels Guldager, Senior Technology Partner, NNE PHRAMAPLAN
KOREA:
How to Bring Global Biopharmaceutical Capability through its Fully-Integrated Production Facilities?
Jeremy Caudill, Global VP Business Development, SAMSUNG BIOLOGICS
SINGAPORE
What do Investors Look for When Investing in Biologics Manufacturing?
Steven Lee, Global Head of Biologics Tech Operations & Managing Director, DR. REDDY'S LABORATORIES
INDIA
Developing a Multiproduct Facility for Biosimilars & Engineering & Biomanufacturing of Enzymes for Different Applications
Arvind Mishra, Global Head of Quality & Regulatory & Head of Strategic Business Unit, Biologicals,
CADILLA PHARMACEUTICALS
Ravindra Wagh, Vice President, ZYDUS BIOLOGICS
Rajeev Soni, Senior Manager, R&D, NOVOZYMES
HONGKONG
What are the Experiences & What is the Future for the Investors in the Biomanufacturing Space?
Ramesh Rajentheran, Head of Asian Healthcare Investment Banking, BARCLAYS
Jason Mann, Managing Director, FENEX CAPITAL MANAGEMENT
INDONESIA
Improving Quality Control & Maintenance of Global Biological Product Distribution
Galatia Chandra, Head of Sales & System, Global Operation, KALBE INTERNATIONAL PTE LTD
http://www.biomanufacturing-asia.com
This 3-day event is the meeting place for international and domestic scientists to share case studies and project updates, showcase new techniques and form collaborations that pave the way towards the future of China’s biopharmaceutical industry.
2nd Annual Oncology Asia
Date: 7 – 9 September 2015 | Sheraton Miyako, Tokyo, Japan
www.oncologyasia.com
The 2nd Annual Oncology Asia zeroes in on the latest cutting edge developments in oncology drug discovery and late phase strategies to get oncology drugs to market faster! Under the Drug Discovery track, this conference will discuss latest immune checkpoint inhibitor combinations, preclinical development trends, novel biomarkers and oncology drug development case studies in Asia. Under the late phase track, it will discuss pricing for success, global and regional commercialization case studies, healthcare policy updates and pricing for success.
Find out about the latest drug discovery trends along with latest strategies for global and regional commercialization at the ONLY senior industry gathering focused on advancing cutting edge oncology R&D and commercialization strategies for Asia in Tokyo, Japan!
With the growth and development of the biopharma industry and increasing changing legislations on areas like biosimilars, pediatric drug development and generic drugs in China and East Asia, now is the time for you to bring along your regulatory affairs teams to keep abreast of evolving regulatory environments and requirements at IBC’s 2nd Pharmaceutical Regulatory Summit in China.
http://www.pharmaregulatoryasia.com/
Biopharma Production and Development China 2015 Rita Barry
As the BioPharma industry grows in China and the Asian region, we invite you to be a part of this tremendous growth & development opportunities!
IBC’s Biopharma Development & Production Week in China is THE meeting place for biopharma industry professionals and scientists to get the highest quality and practical information that will enable them to develop competitive advantages and advance their capabilities in developing and manufacturing cell lines, biosimilars, biobetters, vaccines or novel biologics.
Top Reasons Why You Should Participate:
- Establish Business Partnerships with Chinese/Asian drug developers and contract
manufacturers
- Learn technical & practical know how from experiences on the ground in Asia
- Showcase your cutting edge solutions in front of key China/Asian Biopharma
decision makers
http://www.biopharmaproduction.com
In its third year, “PEGS China: Protein and Antibody Engineering & Development Summit” returns to Shanghai for 3 days of inspiring presentations and case studies featuring the latest trends and future potential of China’s biotech industry.
This year’s event comprises four content-driven conferences with over sixty global speakers, plus a new 1-day seminar on clinical & regulatory strategies for global and domestic IND and BLA filings. In addition, dedicated exhibit hall and poster viewing hours will provide invaluable opportunities for networking, deal-making and ideas exchange.
Animal Health Conference China - featuring senior executives from animal heal...Lei Ching Y.
IBC’s Animal Health Conference focuses on the investments, projects, research and partnerships going into the Asian Animal Health Business.
Key Conference Themes:
• Regulation, Trends & Market Opportunities in Asia Pacific
• Animal Health Business Models & Collaboration
• Prevention & Control of Animal Diseases
• Zoonoses, Human-Animal Interaction & Risk Mitigation
• Product Development & Marketing
• Animal Health Vaccines
For more information, visit www.animalhealthconference.com
Factors to keep in mind when you’re considering cloud storage services.Rita Barry
Cloud storage is a broad term. It can encompass anything from on premise solutions, to le storage, disaster recovery and off premise options. To narrow the scope, I’ve dedicated the focus of today’s discussion to the more popular cloud storage services—such as Dropbox, Box, OneDrive—which are also known as hosted, off premise solutions.
More Related Content
Similar to Biopharma Production & Development Week 2015
Why you should attend:
1. Learn from in-depth case studies on strategic partnering and effective collaboration
2. Explore new business opportunities and strategies to reach the biosimilars market in the region
3. Gain insights into the regulatory landscape for biosimilars in China, India, Korea, Taiwan and more
4. Gather the latest market intelligence and analysis and identify new trends and opportunities in Biosimilars R&D, contract manufacturing and commercialization in Asia
报名参加的五大理由
1. 深入学习有关与亚洲公司建立战略合作和有效协作的案例研究
2. 探索新的商机和战略,以便进入当地的生物仿制药市场
3. 深入了解中国、印度、韩国、台湾以及更多国家或地区的生物仿制药监管形势
4. 收集最新的市场情报和分析,确定生物仿制药研发、合同制造和商业化在亚洲的新趋势和机会
Hear about:
Biopharma Regulatory Updates and Development
Victoria Elegant, VP Medical & Regulatory Affairs, Baxter, China
Andrea Laslop, Head of Scientific Office, Austrian Agency for Food and Health Safety, Austrian Member, European Medicines Agency
Arvind Mishra, Global Head of Quality & Regulatory & Head of Strategic Business Unit, Biologicals, Cadilla Pharmaceutical, India
Advances in Biosimilars R&D
Jeffrey Su, CSO, Cytovance Biologics, USA
Wenzhi Tian, CEO, Huabo Biopharma, China
Ming Wang, President and COO, Gan & Lee Pharmaceuticals, China
Feng Li, CEO, Beijing Mabworks, China
Shaligram Rane, Vice President for Quality, Intas Pharmaceuticals, India
Understanding Obstacles and Hurdles for Entering the Biosimilars Market
Khai Meng Ang, Vice President Asia, Hospira, China
Jason Li, Senior Director, Genor Biopharma, China
Sachidananda Moorthy, Vice President - Clinical Research, Medical and Regulatory Affairs, Avesthagen, India
Sameer Agarwal, Senior Vice President, Business Center Strategic Marketing, Business Unit Generic Drugs & Standard Solutions, Fresenius Kabi, Germany
What can Asia Learn from Global Biosimilars Development and Litigation?
Li Cai, Regional R&D Counsel, Pfizer, China
Vivek Mittal, Head – Legal, Lupin, India
Viren Mahurkar, Managing Director, HitechnRock Advisors, Singapore
http://www.biosimilarsasia.com
Pre-Conference Special Focus Day, 20 May 2014
Clinical Development for Biosimilars
Post-Conference Workshops, 23 May 2014
A: Challenges in Demonstrating Biosimilarity and Interchangeability of Biosimilar Products
B: Successfully Bringing Biosimilars to Market
会前特别关注日,2014 年 5 月 20 日
生物仿制药的临床开发
会后研讨会,2014 年 5 月 23 日
A:在展示生物仿制药产品的生物相似性和可互换性方面所面临的挑战
B:成功地将生物仿制药推向市场
What’s NEW in 2015’s program?
• More case studies on successful commercialization
• Insights on developing biosimilars under new CFDA guideline
• Emerging business models in regulated and developing markets
• New and timely topics on:
o Valuating biosimilars investments
o Successful technology transfer
o Key criteria in gaining approval
Also, NEW Expert Faculty includes:
Dr Shin Jae Chang, Vice President, Celltrion, Korea
Ira Jacobs, Global Oncology Lead, Biosimilars, Pfizer, US
Paul Thomas, Business Unit Head – Biosimilars, Biocon, India
Dr. Martina A. Sersch, Global Clinical Lead, Oncology Global Development, APAC Biotherapeutics Lead, Genentech, Inc. / F. Hoffmann-La Roche Ltd.
Raj Kannan, Vice President, Commercial Head, Biosimilars, Merck, Switzerland
Huiguo (Forrest) Hu, General Manager of International Business, Shanghai CP Guojian Pharmaceutical Co., Ltd, China
Ko Chung Lin, Chief Executive Officer, PharmaEssentia Corporation, Taiwan
Wen Yong, Vice Director, Drug Research Institutes, Biopharmaceutical Institute, Jiangsu AoSaiKang Pharmaceutical Co Ltd, China
http://www.biosimilarsasia.com
“A key source of growth in biologics over the next several years will be Biomanufacturing” Ge Li, Chairman and CEO, Wuxi” <outsourcing-pharma.com,>
“Other issues with single-use include standardization of systems, the dependability to vendors, and the supply chain and waste management but if we can overcome extractables and leachables, we will eventually be able to scale up to many thousands of liters.” Jason Li, Senior Director, Downstream Processing, Genor Biopharma <biopharma-reporter.com,>
Industry experts will discuss these and more at the 5th Annual Biomanufacturing Conference in Grand Hyatt Shanghai, China on 19 – 22 May 2015 during IBC’s Biopharma Development & Production (BDP) Week.
Biomanufacturing in China: Technologies and Facility DesignRita Barry
Join us as we DISCOVER, ANALYZE and LEARN the current state of the global biomanufacturing industry and the future growth potential and recent developments in Asia.
Some of the Key Highlights You Won’t Want to Miss Include
USA
Smart & Flexible Manufacturing Solutions in Multi-Product Facilities
Franz Walz, Executive Director Global Manufacturing, Science and Technology & Network Coordination, BOEHRINGER INGELHEIM
EUROPE
MAb Manufacturing Facilities for China & Automated Single-Use Processing to Bring Control & Flexibility to Manufacturing
Pauline Nicholson, Global Product Manager, Allegro Single-Use Systems, PALL
Niels Guldager, Senior Technology Partner, NNE PHRAMAPLAN
KOREA:
How to Bring Global Biopharmaceutical Capability through its Fully-Integrated Production Facilities?
Jeremy Caudill, Global VP Business Development, SAMSUNG BIOLOGICS
SINGAPORE
What do Investors Look for When Investing in Biologics Manufacturing?
Steven Lee, Global Head of Biologics Tech Operations & Managing Director, DR. REDDY'S LABORATORIES
INDIA
Developing a Multiproduct Facility for Biosimilars & Engineering & Biomanufacturing of Enzymes for Different Applications
Arvind Mishra, Global Head of Quality & Regulatory & Head of Strategic Business Unit, Biologicals,
CADILLA PHARMACEUTICALS
Ravindra Wagh, Vice President, ZYDUS BIOLOGICS
Rajeev Soni, Senior Manager, R&D, NOVOZYMES
HONGKONG
What are the Experiences & What is the Future for the Investors in the Biomanufacturing Space?
Ramesh Rajentheran, Head of Asian Healthcare Investment Banking, BARCLAYS
Jason Mann, Managing Director, FENEX CAPITAL MANAGEMENT
INDONESIA
Improving Quality Control & Maintenance of Global Biological Product Distribution
Galatia Chandra, Head of Sales & System, Global Operation, KALBE INTERNATIONAL PTE LTD
http://www.biomanufacturing-asia.com
This 3-day event is the meeting place for international and domestic scientists to share case studies and project updates, showcase new techniques and form collaborations that pave the way towards the future of China’s biopharmaceutical industry.
2nd Annual Oncology Asia
Date: 7 – 9 September 2015 | Sheraton Miyako, Tokyo, Japan
www.oncologyasia.com
The 2nd Annual Oncology Asia zeroes in on the latest cutting edge developments in oncology drug discovery and late phase strategies to get oncology drugs to market faster! Under the Drug Discovery track, this conference will discuss latest immune checkpoint inhibitor combinations, preclinical development trends, novel biomarkers and oncology drug development case studies in Asia. Under the late phase track, it will discuss pricing for success, global and regional commercialization case studies, healthcare policy updates and pricing for success.
Find out about the latest drug discovery trends along with latest strategies for global and regional commercialization at the ONLY senior industry gathering focused on advancing cutting edge oncology R&D and commercialization strategies for Asia in Tokyo, Japan!
With the growth and development of the biopharma industry and increasing changing legislations on areas like biosimilars, pediatric drug development and generic drugs in China and East Asia, now is the time for you to bring along your regulatory affairs teams to keep abreast of evolving regulatory environments and requirements at IBC’s 2nd Pharmaceutical Regulatory Summit in China.
http://www.pharmaregulatoryasia.com/
Biopharma Production and Development China 2015 Rita Barry
As the BioPharma industry grows in China and the Asian region, we invite you to be a part of this tremendous growth & development opportunities!
IBC’s Biopharma Development & Production Week in China is THE meeting place for biopharma industry professionals and scientists to get the highest quality and practical information that will enable them to develop competitive advantages and advance their capabilities in developing and manufacturing cell lines, biosimilars, biobetters, vaccines or novel biologics.
Top Reasons Why You Should Participate:
- Establish Business Partnerships with Chinese/Asian drug developers and contract
manufacturers
- Learn technical & practical know how from experiences on the ground in Asia
- Showcase your cutting edge solutions in front of key China/Asian Biopharma
decision makers
http://www.biopharmaproduction.com
In its third year, “PEGS China: Protein and Antibody Engineering & Development Summit” returns to Shanghai for 3 days of inspiring presentations and case studies featuring the latest trends and future potential of China’s biotech industry.
This year’s event comprises four content-driven conferences with over sixty global speakers, plus a new 1-day seminar on clinical & regulatory strategies for global and domestic IND and BLA filings. In addition, dedicated exhibit hall and poster viewing hours will provide invaluable opportunities for networking, deal-making and ideas exchange.
Animal Health Conference China - featuring senior executives from animal heal...Lei Ching Y.
IBC’s Animal Health Conference focuses on the investments, projects, research and partnerships going into the Asian Animal Health Business.
Key Conference Themes:
• Regulation, Trends & Market Opportunities in Asia Pacific
• Animal Health Business Models & Collaboration
• Prevention & Control of Animal Diseases
• Zoonoses, Human-Animal Interaction & Risk Mitigation
• Product Development & Marketing
• Animal Health Vaccines
For more information, visit www.animalhealthconference.com
Similar to Biopharma Production & Development Week 2015 (20)
Factors to keep in mind when you’re considering cloud storage services.Rita Barry
Cloud storage is a broad term. It can encompass anything from on premise solutions, to le storage, disaster recovery and off premise options. To narrow the scope, I’ve dedicated the focus of today’s discussion to the more popular cloud storage services—such as Dropbox, Box, OneDrive—which are also known as hosted, off premise solutions.
Unlike more tangible technologies where a failed implementation causes a down network, SIEM (security information and event management) requires a more qualitative approach to determining success or failure. The surprising reality is that most SIEM projects completely fail to deliver any discernable bene ts to the organization and are abandoned in frustration
www.rkon.com
Carve-outs and Mergers and Acquisitions place unique demands on IT. How can y...Rita Barry
Mergers are complex and Carve-outs only add to the dif culty and the level of complexity that the delivery team must manage. The creation of a stand-alone entity in a matter of weeks is daunting; moreover, the lack of cooperation from the legacy organization or the attrition of employees creates a chaotic environment that must be overcome. RKON helps clients to determine the most favorable level of IT sourcing and to implement the most appropriate technology for the new business unit — all to ensure a successful “day one.”
Tertiary Hospital Services Asia 2015, part of the Asia Healthcare Summit, will examine successful case studies on achieving top financially performing healthcare organizations whilst delivering quality tertiary healthcare services.
Top Industry Issues to Be Discussed Include:
Benchmarks and lessons from World Class Tertiary Hospitals
Insights on clinical and operational excellence
Investment in Tertiary Hospital Services and achieving financial success
Streamlining outpatient services
Advanced consultative care & remote monitoring of patient health
Latest technology transforming patient accessibility, care and experiences
Keynote representatives and decision makers from more than 15 public and private hospitals across the Asia Pacific region will convene and share their perspectives in developing world class tertiary hospital services, including:
Chan Choo Lin, Director of Operations, Johns Hopkins, Singapore
Dr. Alejandro C. Dizon, Chief Quality Officer, St. Luke's Medical Center, Philippines
Alastair Mah, Chief Medical Officer, University Hospital Geelong & Barwon Health, Australia
Haji Abdul Aziz Abdul Rahman, CEO, KPJ Penang Specialist Hospital, Malaysia
Seemant Jauhari, CEO, Research & Innovations, Apollo Hospitals, India
Nguyen Thi Le Thu, Marketing & Business Development Director, FV Hospital, Vietnam
Grace Siew Wah Lim, Chief Financial Officer, KK Woman’s and Children’s Hospital, Singapore
Andres M.Licaros, Jr., President & Chief Executive Officer, Asian Hospital and Medical Center, Philippines
Michael Wong, CEO, Pantai Hospitals (Ayer Keroh), Malaysia
David Sun, Consultant of Neurosurgery, Prince of Wales Hospital, Hong Kong
Joe Hau, Director Corporate Services, Tan Tock Seng Hospital, Singapore
Alan Young, Head of IT, Canossa Hospital (Caritas), Hong Kong
Prof Kazuhiro Hara, President, Japanese Telemedicine and Telecare Association, Specially-appointed professor of Seto Inland Sea Regional Research Center, Kagawa University, Japan
Chan Woo Kuk, Center for Future Innovation, Advisory Specialist, Samsung Medical Center, Korea
http://www.tertiaryhospitalservices.com
As you know, pharma compliance is a critical issue, particularly in China. The Chinese government’s recent crackdowns on the business practices of various pharmaceutical companies have sent shockwaves throughout the industry and the price to pay for non-compliance is exceedingly high, with massive revenue losses and irreclaimable reputational damages
To address this pertinent issue, IBC Asia is convening the forthcoming Pharma Compliance Summit
(Mar 2015) in Shanghai, China. Set to be an informative and insightful event, this conference will prepare participants in dealing with the latest legal compliance landmines and equip them with an in-depth understanding of how to mitigate non- compliance risks at every part of the pharma value chain.
Top companies will share best practices of internal compliance programs and third party due diligence strategies; Gain these exclusive insights and incorporate them into their own company, reaping maximum benefits.
Your expert speaker faculty includes:
• Leon Wang, Vice President, AstraZeneca China
• Heike Deters, Head of Compliance, Bayer Healthcare China
• Dr Wang Xianlin, Member, Expert Advisory Group of Anti-Monopoly Commission, State Council People’s Republic of China
• Maija Burtmanis, Regional Legal & Compliance Director JAPAC, AbbVie
• Gareth Lee, General Counsel & Head of Compliance APAC, Allergan
• Cristopher Landrito, Regional Compliance Manager APAC, Merck
• David Shen, General Counsel & VP Legal, AstraZeneca China
• Dr Wu Ke, President, Shanghai BravoBio
• Alejandro Castro, Regional Audit Manager Asia Pacific, Novartis
• Linda Ling, Senior Healthcare Compliance Manager, OTC China, Johnson & Johnson
http://www.pharmacompliance-china.com
IBC’s OTC Pharma Asia conference is returning 2-5 March 2015 at Grand Copthorne Waterfront Hotel, Singapore to prepare you for future growth in the OTC and Consumer Health market in Asia. You will witness how the OTC landscape varies by country as well as the latest product trends, consumer insights and innovative offerings in OTC – a crucial element to achieve global success.
http://www.otcpharmaasia.com
The inaugural Philippines Healthcare will focus on investment opportunities in the Philippines healthcare sector as well as examine the developments in healthcare plans and policies by government, market access opportunities for pharma and technology, new healthcare facility projects, upgrades and expansions and increasing efficiencies of existing facilities.
Philippines is currently focused on speeding up health facilities and upgrades, meeting the needs and growing demand for health specialists, training to ensure competency and quality of healthcare services and ensuring the availability of drugs throughout the country.
The conference will have discussions on policy and regulation updates, investment opportunities, projects and developments to strengthen Philippines healthcare infrastructure and delivery.
It will be held in Manila and will have representations from government, hospitals, insurance companies, pharma companies, health technology and medical device providers and other related stakeholders.
For 2015, we are going to hear NEW panel speakers from Indonesia Stock Exchange, Australia Stock Exchange, Philippine Stock Exchange, Tokyo Stock Exchange, Osaka Stock Exchange and Colombo Stock Exchange. Each of the exchanges will present a 10 minute update about their country on what are the new initiatives that have rolled out, how they address the needs of the private side, which infrastructure support the local regulatory body address in the short term vs. long term and the ASEAN trading link to ease cross border trading.
Not only that, we will answer key questions of the post trade industry including:
• Have Asian market participants been preparing for operational readiness as Dodd Frank, Emir and Basel 3 are being unrolled in Asia?
• Will T2S lead to a migration of all financial players to ISO 20022 in Europe?
• What are the impacts of Hong Kong Shanghai Stock Connect on Asia’s economy and the global financial markets?
• What is the impact on transaction funding and foreign exchange operations of moving from T+3 to T+2?
• Are CCPs all equal? Can we quantify the benefits of moving to a CCP?
• How is the buyside firm in Asia dealing with a collateral solution? Do the costs outweigh the benefits?
With cancer being the fastest growing healthcare priority in the pharmaceutical industry, IBC Asia announces the region's first ever strategic oncology conference focusing on clinical development and market access.
Download the brochure <link> now to identify new trends and opportunities in development and commercialization in the region.
ONCOLOGY ASIA focuses on the clinical development and effective market access for cancer drugs in Asia. It will cover strategies for developing oncology products and businesses from innovative pipelines, commercializing products, sales and marketing strategies to capture opportunities in Asia’s markets.
Featured sessions from top industry thought leaders:
Market Trends and Drivers in the Region
• James Garner, Head Unit Development Operations, Asia R&D, Sanofi, Singapore
What You Need to Know When Marketing Oncology Drugs
• Dr Paul Cornes, Clinical Oncologist, Bristol Oncology Centre, UK
Successful Market Access Strategies for Oncology Drugs
• Sameer Agarwal, Senior Vice President, Business Center Strategic
Marketing, Fresenius Kabi Deutschland GmbH, Germany
Clinical Engagement for Successful Oncology Products
• Dr Anish Desai, Director Medical & Clinical Affairs, Johnson & Johnson, India
http://www.oncologyasia.com
The offshore RMB market has evolved rapidly since 2010 and there have been periods of significant pricing dislocation between onshore and offshore forex and interest rate markets. Over the medium to long term, as the RMB exchange rate becomes more flexible, more products are traded in the offshore RMB market with growing liquidity, and capital account is gradually liberalized, the convergence trend in the pricing of onshore and offshore RMB asset markets is inevitable. <China Money Network, 28 July 2014)
The Value of RMB Currency in the Market, Liquidity & Risk will be discussed at IBC’s Offshore RMB Seminar (Parkroyal on Beach Road, Singapore * 27 November 2014) by these industry leaders:
Joe Ng, Head of Renminbi Payments Product Management - Asia Pacific, Global Transaction Banking, Deutsche Bank, Hong Kong
Update Speaker from Gladys, ICBC, Singapore
Motasim Iqbal, Head of Transaction Banking, Standard Chartered Bank, Singapore
Noritaka Akamatsu, Deputy Head, Office of Regional Economic Integration, Chair, Financial Sector Community of Practice, Asian Development Bank, Philippines
Other Key Topics Addressed Include:
• RMB Policy Liberalization
• Investing in RMB Capital Markets
• RMB Cross-Border Settlements
• Developing of Offshore RMB Operations
View more at http://www.offshorermbseminar.com
A successful generic product starts with understanding consumer needs and brand value. On November 4-7 in Singapore, IBC will host the 9th Annual Generics Asia 2014, Asia’s longest running Generics conference, to help you and your organization understand how to incorporate marketing and partnership into your business strategy.
The key topics to be covered at the event include:
Regulatory Update and Accelerating Access to New market
o A panel of experts from Philippines Chamber of Pharmaceutical Industry, Actavis, Hovid and Pfizer
Building Brand Awareness and Delivering New Products with a Cost Effective Strategy
o Allan Marx Ancheta, Director Business Development and Strategy, Commercial Innovation and Alliance, Merck
Managing Sale Force Effectiveness and Innovative Channels for Generics Products
o Marvin Biliwang, Commercial Effectiveness Director, Takeda Pharmaceuticals
Establishing Partnerships to Add Value and Build Market Share
o Philip Cox, President Director, PT Takeda Indonesia
Innovative Models and Super Generics for Prolonging Product Life Cycles
o Dr. Shirish Kulkarni, Senior Vice President, Formulation Development, Sun Pharmaceutical
IBC’s Indonesia Healthcare conference brings together healthcare leaders to discuss evolving policies, opportunities for private healthcare investment, partnerships, projects and initiatives.
Key Conference Themes:
Updates on Regulation and the Road Towards Universal Healthcare Coverage
Hospital Management & Cutting Edge Healthcare Delivery Standards
Digital Marketing and Telehealth Solutions
Healthcare Infrastructure Projects, Investments & Development
Generics & Access to Medicine
Public-Private Partnerships & Collaboration
Why You Must Attend This Year’s Event
Understand the proactive steps to take by hospitals, pharmaceutical and insurance companies for the new Universal Healthcare Coverage policy
Discover partnerships and investment opportunities in Indonesia
Hear different case studies from major hospitals, insurance and pharmaceutical companies
Meet and exchange business cards with your peers during the networking sessions
Learn how to deliver safe and quality healthcare from other Asian countries
Medical Affairs teams in Asia’s diverse markets need to collaborate with R&D and understand the science, the business and the regulations. They need to constantly think strategically and communicate effectively.
• How can Medical Affairs teams be even more impactful in enhancing your company’s scientific reputation?
• How can you better communicate the value of your products to KOLs and Healthcare professionals?
• What makes a successful Medical Affairs team in Asia?
Get the answers and more at the 3rd MEDICAL AFFAIRS FORUM ASIA {link} - the region’s longest running strategy forum where leading medical affairs professionals share best practices, discuss common issues and learn from industry experts to enhance scientific reputation and better communicate the value of products to KOLs.
http://www.pharmaconasia.com/medical-affairs-forum-asia
PharmaCon - Pharmaceutical Congress Asia 2014 Rita Barry
The Leading Event Bringing 4 Successful Events Under 1 Roof!
The Pharmaceutical Congress Asia recognizes the importance of strong partnerships to drive innovation, development and winning products and services in Asia’s growing pharmaceutical industry. Packed with case studies from market leaders, four agendas will unite to create a hub of research, innovation, improved regulatory frameworks, best practice business, marketing and distribution models that will define Asia’s pharmaceutical future.
http://www.pharmaconasia.com
The Most Comprehensive Coverage of China’s Evolving Biologics Market
________________________________________
20 Case Studies ● Keynote from China SFDA Official
17 New Data Presentations ● Panel Discussions on Biosimilar and Analytical Methods
• Harness novel cell line technologies and approaches for improved developability and upstream processing
• Enhance analytical capabilities with new characterization and specification methods
• Benchmark your biosimilar program with case studies and new data on development and production
• Meet complex drug product and manufacturing challenges with new facility technologies and designs
http://www.ibclifesciences.com/bpichina
We’re pleased to announce that the Conference and Workshop programme for ISPE Singapore is ready to view on www.ispesingapore.org
FINAL BROCHURE NOW AVAILABLE FOR DOWNLOAD HERE!
This year, you’ll find:
• 90% NEW & 50% MORE Speakers than in 2013
• Over 34 presenters sharing their case studies and experience
• Choose from 36 hours of Learning, 6 hours of Networking Across the Plenary Conference & 9 practical workshops
• The latest solutions at the ISPE Singapore Exhibition on 23-24 June
• And don’t forget to sign up for the Site Visit to MSD Singapore Plant Extension!
Build your own agenda from 3 concurrent sessions:
Sunday 22 June (1.30-5.30pm):
A: Quality / Validation
B: Operational Excellence
C: Bio / Sterile / Clean Utilities
Monday 23 June (2.00-5.45pm):
D: Tech Transfer / Process Validation
E: QBD / PAT
F: Sterile Operations
Tuesday 23 June (9.00-3.30pm):
G: Quality / Audit / Regulatory
H: Operational Excellence / Lean Manufacturing
J: Biologics
‘’Healthcare providers are aware of the long-term cost benefits of cloud solutions; what they are looking for now are reliable technology partners who can address their concerns over data privacy and security. ‘’ –Pharmatimes, October 2013
Select your dream technology partner this 4th Electronic Health records!
With our Open Sharing session on EHR technology, YOU get the chance to voice your thoughts out or hear from our speakers and attendees their experiences with various vendors and learn from their challenges faced and select the RIGHT EHR technology which suits your needs!
In addition, don’t miss our brand new sessions on EHR’s data privacy & security & its data protection laws!
Introducing our panel of expert speakers!
Jovita Aragona, Information Technology Officer III, Department of Health, Philippines
Johan A. Hutauruk, IT Director, Jakarta Eye Centre, Indonesia
Md. Khadzir b Sheikh Haji Ahmad, Deputy Director, Health Informatic Centre, Ministry of Health, Malaysia
Suresh Poonudurai, CEO, Malaysian Healthcare, Malaysia
Stephen Chu, Chief Clinical Informatician & Terminologist, NEHTA, Australia
Robert P. Jalleh, Chairman, Alpha Specialist Centre, Malaysia
Marc Hsu, Director, Medical Informatics Centre, Ministry of Health and Welfare, Taiwan
Bryan Tan, Partner, Pinsent Mason Mpillay, Singapore
www.electronichealthasia.com
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
Adv. biopharm. APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMSAkankshaAshtankar
MIP 201T & MPH 202T
ADVANCED BIOPHARMACEUTICS & PHARMACOKINETICS : UNIT 5
APPLICATION OF PHARMACOKINETICS : TARGETED DRUG DELIVERY SYSTEMS By - AKANKSHA ASHTANKAR
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
1. 19 — 22 May 2015
Grand Hyatt Shanghai, China
IBC
LIFE SCIENCES
4th ANNUAL 5th ANNUAL 6th ANNUAL
Produced by:
www.biopharmaproduction.com
STILL the Leading Series in China with
Quality Content & a Strong Following of Top
Pharma & Biotech Stakeholders!
Yariv Hefez
Vice President Business
Development, Portfolio
Management, Strategy and
Partnering, Biosimilars Unit,
Merck, Switzerland
Richard O’Keeffe
Executive Director,
InternationalQuality–Japan-
Asia-Pacific (JAPAC) Regional
Quality Head,
Amgen, Singapore
Shou-Bai Chao
Senior Vice President, Bio
Ventures, Global Operations,
AstraZeneca, China
Lin Hong
Associate Director,
RegulatoryAffairs,AsiaPacific
Russia CIS (APAC),
Abbott, USA
Dr Ira Allen Jacobs
Oncology Portfolio Global
Medical Lead-Biosimilars,
Pfizer, USA
Dr. Martina A. Sersch
Global Clinical Lead, Oncology
Global Development, APAC
Biotherapeutics Lead,
Genentech, Inc. /
F. Hoffmann-La Roche Ltd.
Abdullah Baaj
CEO,
Boston Oncology, USA
Lars Dreesmann
Executive Director Upstream
Manufacturing & Tech
Transfer H84 & PT&PE H84,
Boehringer Ingelheim
Pharma, Germany
David Shen
Vice President,
NGMBiopharmaceuticals,
USA
Raj Mehta
President – Biotech,
Cadila Pharaceuticals Ltd,
India
Scott Liu
President & CEO,
Henlius Biopharmaceuticals,
USA
Li Shi
CEO,
Shanghai Zerun
Biotechnology, China
Pengfei Zhou
CEO,
Wuhan YZY Biopharma
Co Ltd, China
Our Distinguished Speaker Line Up
What’s New
for 2015
C-Level Panel: Cutting Edge
Insights on China’s Growing
Biotech Market
China FDA Special Address
80+ Key Expert Speakers from
Asia’s leading Pharma & Biotech
1 Joint Exhibition & Networking
Area
4 Days of Expert Knowledge
Sharing
Revamped Program with New
Special Focused Tracks &
Sessions
EXCLUSIVE
SITE TOUR!
Boehringer Ingelheim’s
New Biopharmaceuticals
Facility-Shanghai China
Peng Wang
President of R&D,
Yabao Pharmaceutical
Group, China
Life
Sciences
2. 08:00 Registration Opens & Morning Coffee
08:50 Welcome Address from IBC Asia
Ice Breaker: Exchange Business Cards & Get to Know Industry
Peers
09:00 Chairperson’s Opening Remarks
Abdullah Baaj, CEO, Boston Oncology, USA
09:10 Keynote Panel: Global Biopharma Outlook: Opportunities &
Challenges 2015 & Beyond
Moderator:
Yariv Hefez, Vice President Business Development, Portfolio
Management, Strategy and Partnering, Biosimilars Unit, Merck,
Switzerland
Panelists:
Abdullah Baaj, CEO, Boston Oncology, USA
Racho Jordanov, President & CEO, JHL Biotech, Taiwan
Richard O’Keeffe, Executive Director, International Quality – Japan-
Asia-Pacific (JAPAC) Regional Quality Head, Amgen, Singapore
Choose Your Own Sessions from 3 Different Tracks
4th ANNUAL
5th ANNUAL
6th ANNUAL
11:30 Chairperson’s Opening Remarks
Pengfei Zhou, CEO, Wuhan YZY Biopharma
Co Ltd, China
Chairperson’s Opening Remarks
Lin Hong, Associate Director, Regulatory Affairs,
Asia Pacific Russia CIS (APAC), Abbott, USA
Chairperson’s Opening Remarks
Dr Ira Allen Jacobs, Oncology Portfolio Global
Medical Lead-Biosimilars, Pfizer, USA
11:40
Efficient Screening Strategies to Select
Clones & Reduce Timelines
Chaomei He, Principal Scientist, Momenta
Pharmaceuticals, USA
Advances in Clone Screening &
Selection
Flexible Facilities & New
Biomanufacturing Technologies
Biosimilars Market Landscape
Fast-Tracking an Efficient Upstream Process
Transfer & Scale up of Biopharmaceutical
Processes
Lars Dreesmann, Executive Director Upstream
Manufacturing & Tech Transfer H84 & PT&PE H84,
Boehringer Ingelheim Pharma, Germany
Biosimilars on the Horizon: Opportunities
and Challenges
Dr Ira Allen Jacobs, Oncology Portfolio Global
Medical Lead-Biosimilars, Pfizer, USA
Analytical Strategies for Increased
Quality in Bioproduction
12:10
High-Throughput (HTP) Analytical Platforms
to Assess Product Quality Attributes in
Cell Lines
Senior Representative, Lonza
Hybrid MAb Facilities: Combining Single Use
Technology & Stainless Steel for China MAb
Facilities
Niels Guldager, Senior Technology Partner, NNE
Pharmaplan, Denmark
FindingSymbioticPartnershipstoAccelerate
Biosimilars Market Launches
Huiguo (Forrest) Hu, General Manager of
International Business, Shanghai CP Guojian
Pharmaceutical Co., Ltd, China
12:50
Networking Lunch & VIP Tables
VIP Table 1: Robin Tan, Head of Analytical Technologies, Shanghai CP Guojian Pharmaceutical, China
VIP Table 2: Shou-Bai Chao, Senior Vice President, Bio Ventures, Global Operations, AstraZeneca, China
VIP Table 3: Michelle Yu Xia, Chairman, President & CEO, Akeso Biopharma, China
VIP Table 4: Paul Thomas, Business Unit Head – Biosimilars, Biocon, India
VIP Table 5: Dr Jiang WeiDong, Chief Science Officer and Vice President, Henlius Biopharmaceuticals, USA
VIP Table 6: Huiguo (Forrest) Hu, General Manager of International Business, Shanghai CP Guojian Pharmaceutical Co., Ltd, China
VIP Table 7: Peng Wang, President of R&D, Yabao Pharmaceutical Group, China
VIP Table 8: Zou Ping, Vice Director, Shanghai CPGJ Pharma, China
VIP Table 9: John Xu, CSO, Shanghai Benemae Pharma & VP, Shanghai Mabicine, China
Exchange business cards and have
an informal chat with key experts
during the networking lunch!
Roundtable Discussions
Each leader will facilitate the discussion for 45 minutes. Leaders will then share key takeaways on the stage for 5 minutes each.
Choose your table now! Email Gladys.Landicho@ibcasia.com.sg
2:30
Roundtable 4: GMP Regulation
Lin Hong, Associate Director, Regulatory Affairs,
Asia Pacific Russia CIS (APAC), Abbott, USA
Roundtable 5: Quality by Design
Kevin Zen, Senior Manager, Biologics
Development, Allergan, USA
Roundtable 6: R&D Investment &
Development
Fei Jiang, Director, Business Development,
3SBio, China
09:45 CEO Panel: Cutting Edge Insights into China’s Growing Biotech
Market
Moderator:
Shou-Bai Chao, Senior Vice President, Bio Ventures, Global Operations,
AstraZeneca, China
Panelists:
Joe Zhou, CEO, Walvax Group, China
Li Shi, CEO, Shanghai Zerun Biotechnology, China
Michelle Yu Xia, Chairman, President & CEO, Akeso Biopharma, China
Scott Liu, President & CEO, Henlius Biopharmaceuticals, USA
10:20 Government Address: China’s Evolving Biopharma Policies &
Regulations
Senior Representative, China Food and Drug Administration (CFDA),
China
10.45 Morning Networking & Refreshment Break
Roundtable 7: Emerging InvestmentTrends
in Biosimilars and Portfolio Management
James Huang, Managing Partner, KPCB, China
Roundtable 8: Bringing Biosimilars to the
Market
DrVilloo Patell, Founder, Chairperson and CEO,
Avesthagen, India
Roundtable 9: Regulatory Pathway in China
ShaoyuChen, Partner;ManagingDirector,China
Food and Drug Practice, Covington & Burling
LLP, China
Roundtable 1: Novel Cell Line Development
and Bioprocess Approaches for Increased
Speed, Titer and Product Quality
Cheng Zhang, CSO, Gmax Biopharm, China
Roundtable 2: Strategies on Raw Material
and Supplier Management for Efficient, Cost-
effective Biopharmaceutical Production
Chiali Liu, Manager, Microbial and Cell Culture
Development, GSK, USA
Roundtable 3: Applying Essential QbD
concepts in Cell Culture and Bioprocess
Deveopment for Biopharmaceuticals
Hung Fai Poon, Director, Cell Culture, Hisun
3:30
CONFERENCE DAY ONE 20 MAY 2015 WEDNESDAY
4:00 Integrating Multi-Omics Analysis & in silico
Modelling of CHO cells for Enhancing Cell
Culture Performance and Product Quality
Dong-Yup Lee, Assistant Professor, Department
of Chemical and Biomolecular Engineering, NUS
Commercialization & Scale - Up
Strategies
Case Study: Manufacturing Complex
Biosimilars
Hui Hu, Vice Director, CPGJ Research Institute,
Shanghai CP Guojian Pharmaceutical, China
Update on Biosimilars Regulations &
Guidelines
Case Study: Developing Biosimilars under
CFDA Guideline
WenYong, ViceDirector,DrugResearchInstitutes,
Biopharmaceutical Institute, Jiangsu
AoSaiKang Pharmaceutical Co Ltd, China
Customer Service Hotline +65 6508 2401 register@ibcasia.com.sg www.biopharmaproduction.com
Afternoon Networking & Refreshment Break
Biopharma Visionary Keynote Sessions
Novel ‘Omics Approaches for
Enhanced Quality’
3. 4:40
Cell Culture Media for
Optimized Growth
Individual Optimization of Chemically
Defined Media
ChuanHe, ProcessDevelopment,SeniorScientist,
Beijing Mabworks Biotech, China
Panel Discussion: Overcoming Challenges of
Scale-Up: Moving Strains from Bench to
Large-Scale Fermentation & Product Recovery
Panelists:
Lei Sun, Vice President, Technology and
Manufacture, AutekBio, China
Weidong Jiang, Chief Scientific Officer and Senior
Vice President, Shanghai Henlius Biotech, China
Hung Fai Poon, R&D Director, Cell Culture, Hisun
Pharmaceutical, China
Regulatory Challenges and Development in
the US and Europe
AndreaLaslop, HeadofScientificOffice,Austrian
Agency for Food and Health Safety, Austrian
Member, European Medicines Agency
5:15
Case Study: Key Criteria in Developing and
Gaining Approval in Biosimilars
Dr Shin Jae Chang, Vice President, Celltrion,
Korea
High Throughput & High Resolution
Glycosylation Analysis Throughout
Bioprocess Development for Improved
Quality
Dr Zhang Peiqing, Research Scientist,
Bioprocessing Technology Institute, A*Star
Singapore
5:50 Chairperson’s Summary
Networking Cocktail
VIP 1: Eric Morfin, Senior Director, Project Management and Operational Excellence, Allergan Biologics, USA
VIP 2: Lin Hong, Associate Director, Regulatory Affairs, Asia Pacific Russia CIS (APAC), Abbott, USA
VIP 3: Michael Grogan, Head of International Logistics & Distribution, Technical Operations, Shire Pharmaceuticals, Ireland
VIP 4: Dr Vivek Mittal, Head – Legal, Lupin, India
VIP 5: David Shen, Vice President, NGM Biopharmaceuticals, USA
VIP 6: Raj Mehta, President – Biotech, Cadila Pharaceuticals Ltd, India
VIP 7: Scott Liu, CEO, Henlius Pharmaceuticals, USA
VIP 8: Feng Tian, Head and Director, Ambrx China
VIP 9: Wen-Chen Suen, Chief Scientific Officer, Biologics Division, HEC Pharm, China
6:00
Exchange business cards and have
an informal chat with key experts
during the networking cocktail!
7:00 End of Conference Day One
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9:00
9:10
Novel Cell line Development Platforms
& Expression Systems
9:50
Chairperson’s Opening Remarks
Hung Fai Poon, Director, Cell Culture, Hisun
Pharmaceuticals, China
Chairperson’s Opening Remarks
Lin Hong, Associate Director, Regulatory Affairs,
Asia-Pacific, Russia CIS (APAC), Abbott, USA
Chairperson’s Opening Remarks
Raj Kannan, Vice President, Commercial Head,
Biosimilars, Merck, Switzerland
Analyzing Cell Line Development Platforms
& Amgen Case Study of Novel Expression
Systems
Dayou Liu, Senior Scientist, Amgen, USA
Global Biotech Advances
Case Study: Supply Security & Quality in 21st
Century Biotech
RichardO’Keeffe, ExecutiveDirector,International
Quality – Japan-Asia-Pacific (JAPAC) Regional
Quality Head, Amgen, Singapore
Latest Biosimilars Technology
& Best Practice Tech Transfer
Case Study:Tips for SuccessfulTechTransfers
Dr Joe Xin Hua, Zhou, Chief Executive Officer,
Walvax Group, China
Panel Discussion: Getting the most out of
Stable versusTransient Expression Systems
Panelists:
XiangYang Zhu, CEO, Huaota Biopharm, China
Dayou Liu, Senior Scientist, Amgen, USA
Cheng Zhang, CSO, Gmax Biopharm, China
Disposable & Stainless Steel HybridTechnique
Used for the Implementation of a New Process
Johannes Salzbrunn, Head of GMP Downstream
/ Fill & Finish, Boehringer Ingelheim Shanghai
Pharmaceuticals, China
SMARTTechnologies – More than Evolution
for Biosimilars
Dr Barbara Paldus, CEO, Finesse Solutions,
Inc., USA
Morning Networking & Refreshment Break10:30
CONFERENCE DAY ONE 20 MAY 2015 WEDNESDAY
CONFERENCE DAY TWO 21 MAY 2015 THURSDAY
TRACK A: FACILITIES TRACK B: PRODUCTION
New Projects Process & Quality
11:00
Using Targeted Genome
Engineering to Advance CHO Cell
Technology
Dr Jamie Freeman, Bioproduction
Product Manager, Horizon
Discovery, U.K
Case Study: Defining Specific
Critical Quality Attributes in
Different R&D Processes
Cuihua (Chloe) Liu, Executive Vice
President, Quality & Regulatory
Affair, Alphamab, China
Case Study: New Antibody
Facility in China
Jason Li, Senior Director,
Downstream Processing,
Genor Biopharma, China
Redefining Consistency and
Reducing Risk with Cell Culture
Media and Supplementation
Senior Executive, BD Advanced
Bioprocessing
Choose Your Own Sessions from 4 Different Tracks
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Examining Design Principles when
Transforming to Flexible Biomanfacturing
Facilities
Strategies for Optimising Glycoslation
4. 11:40
Overcoming the‘Position Effect’
– Targeting Integration into
Chromosomal Hotspots for
Rapid Cell Line Development
Yuan Sheng Yang, Senior Staff
Research Scientist, Bioprocessing
Technology Institute, Singapore
Case Study: Building an
AntibodyManufacturingFacility:
Path of a Start-Up Company
Cheng Zhang, Chief Scientific
Technology Officer, Gmax
BioPharm, China
Case Study: Insect Cell-
Baculovirus System for
Innovative Vaccine Production
John Zeng, Executive Vice
President, Product Development
and Clinical Manufacturing,
Shanghai Zerun Biotech,
China
Productive Development
Partnerships (PDP) &
Biosimilar Investments
PDP and the Biosimilar
Opportunity in LATAM
Yariv Hefez, Vice President Business
Development, Portfolio
Management, Strategy and
Partnering, Merck, Switzerland
12:20
Efficient Bioprocess Design
& Scaling Up Strategies
Bioprocess Design Strategies to
Increase Quality and Efficiency
Zhiwei Pan, Senior Director, Cell
Culture Process Development,
Livzon mAbpharm, China
Case Study: Manufacturing &
Applications of Oligonucleotides
for Research, Diagnostics &
Therapeutics in China
Dmitry Samarsky, Executive
Vice President, Technology &
Business Development, RiboBio,
China
Case Study: Production, Quality
Control & Clinical Approval
Process of TK006, A Denosumab
Biosimilar
Yan Shan Huang, Senior Vice
President, Antibody Pharmaceutics,
JiangsuT-mab Biopharma, China
Identifying the Best Investment
Model and Valuating Biosimilar
Opportunities
Dr Patrik Frei, CEO, Venture
Valuation VV Asia, Singapore
1:00
Networking Luncheon & VIP Tables
VIP Table 1: Masih Sabet, Associate Director Quality Assurance, APAC Technology Operation, UCB, China
VIP Table 2: Cuihua (Chloe) Liu, Executive Vice President, Quality & Regulatory Affairs, Alphamab, China
VIP Table 3: Zhonghui Lian, Deputy Chief Engineer, Technical Service Department, Beijing Yizhuang Biomedical Park, China
VIP Table 4: Ko Chung Lin, Chief Executive Officer, PharmaEssentia Corporation, Taiwan
VIP Table 5: Raj Kannan, Vice President, Commercial Head, Biosimilars, Merck, Switzerland
VIP Table 6: Dr. Martina A. Sersch, Global Clinical Lead, Oncology Global Development, APAC Biotherapeutics Lead,
Genentech, Inc. / F. Hoffmann-La Roche Ltd.
VIP Table 7: Pengfei Zhou, CEO, Wuhan YZY Biopharma Co Ltd, China
VIP Table 8: Andy Tsun, Senior Manager & Group Head, Novel Drug and Cell Line Development, Innovent Biologics, China
VIP Table 9: Xiang Yang Zhu, CEO, Huaota Biopharm, China
Bring your questions
and visit the
guests during the
networking lunch!
2:00
Biomanufacturing Project
Design & Planning
Efficient Cell Culture Process
Development & Case Study of
Single-use Bioreactors
Hao Chen, Principal Scientist,
Merck, USA
Best Practices for Executing
Seismically Safe Medical New
Facilities
Eric Morfin, Senior Director, Project
Management and Operational
Excellence, Allergan Biologics, USA
Successfully Applying Quality
by Design (QbD) Concepts to
Develop a Robust Protein
Therapeutic Formulation
Kevin Zen, Senior Manager,
Biologics Development,
Allergan, USA
Market Access and
Commercialization
Case Study: Developing
Biosimilars/Biobetters in
Emerging and Regulated
Markets
Ko Chung Lin, Chief Executive
Officer, PharmaEssentia
Corporation, Taiwan
2:40
Biomanufacturing
Finance & Investment
Technology Transfer &
cGMP
Developing a Strategy for
Successful Scale Up
Chiali Liu, Manager,
Microbial and Cell Culture
Development, GSK, USA
Case Study: Financing &
Investing in Biomanufacturing
Facilities in China
Peter Fuhrman, Chairman & CEO,
China First Capital, China
Case Study: EfficientTechnology
Transfer in Asia Whilst
Complying with cGMP
Xiaoyong(Sam)Wu, OSDTechnical
Lead, AstraZeneca, China
Developing Commercial
Strategies to Optimize Market
Uptake
Raj Kannan, Vice President,
Commercial Head, Biosimilars,
Merck, Switzerland
3:20 Afternoon Networking & Refreshment Break
3:50
Biomanufacturing Supply
Chain Efficiencies
Panel Discussion: Insights into
Next-Generation Bioprocessing
Moderator:
Prof Rolf G Werner, Industrial
Biotechnology Department,
University ofTubingen, Germany
Panelists:
Chiali Liu, Manager, Microbial and
CellCultureDevelopment, GSK, USA
Hao Chen, Principal Scientist,
Merck, USA
Zhiwei Pan, Senior Director, Cell
Culture Process Development,
Livzon mAbpharm, China
Commercial Viability of
Antibody Drug Investment
& Development
Case Study: Distributing
Biologics in Multiple Growing
Markets Efficiently
Michael Grogan, Head of
InternationalLogistics&Distribution,
Technical Operations, Shire
Pharmaceuticals, Ireland
Panel Discussion: Risks and
Opportunities in Biosimilars/
Biobetters and Key Enablers for
Advancement
Moderator:
Salman Bokhari, Managing
Director, Sidrapex, Singapore
Panelists:
Atul Deshpande, Associate
Director, Unit Strategy Office, Asia
Pacific Therapeutic Strategy Unit,
Sanofi, China
PaulThomas, Business Unit Head –
Biosimilars, Biocon, India
Ko Chung Lin, Chief Executive
Officer, PharmaEssentia
Corporation, Taiwan
Tadashi Matsumoto, President/
Chief Executive Officer, Reqmed Co
Ltd, Japan
Green & Energy Efficient
Biomanufacturing Facilities
4:30
Case Study: Going Green in
Biomanufacturing
Case Study: Cold Chain
Management from
Manufacturing to Distribution of
Biologics
Masih Sabet, Associate Director
QualityAssurance,APACTechnology
Operation, UCB, China
Biosimilars Clinical Trials
Development: Key
Considerations in Planning and
Execution
Dr Arun Maseeh, Vice President,
Medical Affairs, Cadila
Pharmaceuticals, India
Clinical
Development
5:10
5:15
Chairperson’s Summary & End of Conference
End of the BDP Week Conferences 2015
CONFERENCE DAY TWO 21 MAY 2015 THURSDAY
TRACK A: FACILITIES TRACK B: PRODUCTION
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Analytical Strategies for Defining
CQA in QbD Bioprocess
Development
Next Generation
Bioprocessing Trends
5. Session 3: Complexity of Monoclonal
Antibodies and Clinical Challenges for
Establishing Biosimilarity
Dr. Martina A. Sersch, Global Clinical Lead,
Oncology Global Development, APAC
Biotherapeutics Lead, Genentech, Inc. / F.
Hoffmann-La Roche Ltd.
Session 4: Proven Scalability of a Predefined
Process in Bringing Biosimilar mAbs to
Market
David Shen, Vice President, NGM
Biopharmaceuticals, USA
BestPracticesinProcessTechnologyTransfer
and cGMP Manufacturing
Hao Chen, Principal Scientist, Merck, USA
Exclusive SiteTour to Boehringer Ingelheim’s
New Biopharmaceuticals Facility in Shanghai,
China
PRE-CONFERENCE WORKSHOPS 19 MAY 2015 TUESDAY
POST-CONFERENCE WORKSHOPS 22 MAY 2015 FRIDAY
9.30am–12.30pm
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Customer Service Hotline +65 6508 2401 register@ibcasia.com.sg www.biopharmaproduction.com
Workshop A Workshop A Special Focus Day A
Monoclonal Antibodies (Mabs)
Session 1:Trends, Challenges and Strategies
for Biosimilar Therapeutic Antibody
Development
Dr Sunit Maity, AVP – Product Development,
Theramyt Novobiologics Private Limited,
India
Session 2: Next Generation of Mabs
Jinming Gu, Senior Scientist, AbbVie
Bioresearch Center, USA
Achieving Operational Excellence in
Bioprocessing: Design of Experiments (DoE)
applications for Cell Culture
Hung Fai Poon, R&D Director, Cell Culture
Hisun Pharma (Hangzhou), China
Boehringer Ingelheim Biopharmaceuticals
Move to China - Operational Excellence and
Experience in 30 years Commercial
Manufacturing
Dr. Jian Huang, Director, Business Development
& Key Account Management, Boehringer
Ingelheim Biopharmaceuticals, China
12.30pm – 1.30pm Networking Lunch
1.30pm–5.00pm
4th ANNUAL
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Special Focus Day C Workshop B Workshop B
Special Focus Day (Continued)
9.30am–12.30pm
Chairperson’s Opening Remarks
Weidong Jian, CSO & VP, Henlius
Biopharmaceuticals, USA
Strategies for Novel Antibodies and
Biosimilars Development
Pei Ye, Vice President, Beijing Mabworks
Biotech, China
Novel Methods in Antibody Discovery and
Characterization
Weidong Jian, CSO & VP, Henlius
Biopharmaceuticals, USA
Strategies in Cell line engineering of
Bi Specific Antibodies
Pengfei Zhou, CEO, Wuhan YZY Biopharma
Co Ltd, China
Boosting Productivity and Efficiency of
Biotherapeutics
Prof Rolf G Werner, Industrial Biotechnology
Department, University ofTubingen, Germany
Crafting Successful Market Access
Strategies for Biosimilars in Emerging
Markets
Salman Bokhari, Managing Director,
Sidrapex, Singapore
Best Corrective & Preventive Action (CAPA) &
Root Cause Analysis Practices for
Biomanufacturing Excellence
Eric Morfin, Senior Director, Project Management
and Operational Excellence, Allergan Biologics,
USA
12.30pm – 1.30pm Networking Lunch
Gaining Approval for Biosimilars in the US
and Europe
Dr. Onesmo Mpanju, Principal Consultant,
Independent Biopharmacuetical Product
Development Consultant, Former Review
Scientist of FDA
Alan Liss, ConsultanttoPharmaceuticalIndustry,
Former Review Scientist of FDA, USA
Novel Strategies in Monoclonal Antibodies
Targeting GPCRs
Cheng Zhang CSO, Gmax Biopharm, China
Strategies in Fc Effector Function Analysis
in Antibodies
Jingyi Xiang,Head of Bioanalytics, Eureka
Pharma, USA
Engineering of Antibody Drug Conjugates
(ADCs) technologies
Chairman Closing Remarks and End of
Post-Conference Special Focus Day
Best Corrective & Preventive Action (CAPA) &
Root Cause Analysis Practices for
Biomanufacturing Excellence (Continued)
Eric Morfin, Senior Director, Project Management
and Operational Excellence, Allergan Biologics,
USA
1.30pm–5.00pm
Add Value to Your Learning with
Interactive Workshops, Focus Days &
a Site Tour to Choose From!
Site TourWorkshop B
Special Focus Day C (Continued) Workshop B (Continued) Workshop C
6. 19 — 22 May 2015
Grand Hyatt Shanghai, China
IBC
LIFE SCIENCES
4th ANNUAL 5th ANNUAL 6th ANNUAL
IBC’s Biopharma Development & Production
Week is the leading industry platform for
pharma, biotech, CMOs, CROs, research
institutes, investors and industry stakeholders
to meet, network and discuss current industry
trends, establish business partnerships and be
updated on investment opportunities in China
and surrounding Asia.
GEOGRAPHY
■ China 50%
■ Rest of North Asia 15%
■ Southeast Asia & India 10%
■ Europe 10%
■ US 10%
■ Rest of the World 5%
Who Shoud Attend
Chairman/Chief
Executive Officer
Chief Operations
Officer
Chief Scientific Officer
Chief Technology
Officer
Chief Marketing Officer
Senior Vice President
Vice President
Biologics
Vice President
Biosimilars
Vice President of R&D
Vice President of
Manufacturing
Vice President of
Facilities
Head of Cell Line
Development
Principal Scientist
Head Process
Development
General Manager
Director
Business Development
Sales & Marketing
Manager
INDUSTRY
■ Pharmaceuticals/Biotech
50%
■ CMOs 15%
■ CROs 15%
■ Technology & Solution
Providers 10%
■ Finance/Law 10%
Abundant
Networking Opportunities
& Interactive Formats
80+ Top Level Speakers
New Pre & Post Workshops
5+ Interactive Panel Discussions
Hot Topic Round Table Discussions
Meet the Experts Via Specially Hosted VIP Lunch Tables
Speed Networking Sessions to Get to Know Your Peers
Conference Networking Cocktail
3 Co-located events under one roof
• 4th Annual Cell Line Development &
Engineering
• 5th Annual Biomanufacturing
• 6th Annual Biosimilars Asia
Revamped program including special focused
tracks on:
• Biomanufacturing Facilities
• Biomanufacturing Production
• Monoclonal Antibodies
• Cutting Edge Trends in Antibody Development
Special Site Tour & Workshop to Boehringer Ingelheim’s new biopharma
facility
Establish Business Partnerships with local Chinese drug developers and
contract manufacturers
Learn technical & practical know how from experiences on the ground in Asia-
Pacific
Showcase your cutting edge solutions in front of key China/Asian Biopharma
decision makers
Speed Networking to get to know your industry peers
Top Reasons Why You
Should Participate:
3SBio • Abbott • AbbVie Bioresearch Center • Agilent Technologies • Akeso Biopharma • Allergan • Allergan Biologics • Alphamab • Ambrx China • Amgen • Anitia OíConnor Consulting
• Astrazeneca • Autekbio • Avesthagen • BD Advance Bioprocessing • Beijing Mabworks Biotech Co Ltd • Beijing Yizhuang Biomedical Park • Biocon • Bioprocessing Technology Institute
• Boehringer Ingelheim Biopharmaceuticals • Boehringer Ingelheim Pharma • Boehringer Ingelheim Shanghai Pharmaceuticals • Boston Oncology • Cadila Pharmaceuticals • Celltrion
• China First Capital • Covington & Burling LLP • CPC • CPGJ Pharma • Eureka Therapeutics, Inc. • European Medicines Agency • FDA • FEF • Finesse Solutions, Inc • Genentech, Inc. / F.
Hoffmann-La Roche Ltd. • Genscript • Genor Biopharma • Gmax Biopharm • GSK • Hanwha Chemical • Henlius Biopharmaceuticals • Hisun Pharma (Hangzhou) Co Ltd • Hisun Pharmaceutical
• Horizon Discovery • Huaota Biopharm • Innovent Biologics, Inc. • JHL Biotech • Jiangsu AoSaiKang Pharmaceutical Co Ltd • Jiangsu T-mab Biopharma • JS Biosciences • JX Nippon Oil
& Energy • KPCB • Livzon mAbpharm • Lonza • Lupin Limited • MedImmune • Merck • Momenta Pharmaceuticals • NGM Biopharmaceuticals • NNE Pharmaplan • NUS • Pfizer • PharmaEssentia
Corporation • Reqmed Co Ltd • RiboBio • Shanghai Benemae pharma • Shanghai CP Guojian Pharmaceutical • Shanghai Henlius Biotech • Shanghai Zerun Biotechnology • Shen Zhen
DongYangGuang Industry Co, HEC R&D Centre • Shire Pharmaceuticals • Sidrapex • Solentim • Theramyt Novobiologics Private Limited • UCB • University of Tubingen, Germany • Venture
Valuation VV Asia • Walvax Group • Wuhan YZY Biopharma Co Ltd • Yabao Pharmaceutical Group • Yong Loo Lin School of Medicine, NUS
The Following Companies Have Already Confirmed their Attendance!
Here’s What Past Attendees Have to Say!
“Valuable, world-class and professionally-organized, this conference was
among the very best I’ve ever attended.”
Peter Fuhrman, Chairman & Chief Executive Officer, China First Capital
“It is a great opportunity to learn biomanufacturing in China.”
Kang Li, Head of Biologics, Beigene
“Very insightful conference with a broad range of issues discussed and
excellent speakers.”
Ramesh Rajentheran, Managing Director, Head – Asian
Healthcare, Investment Banking, Barclays
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7. Exhibitor
Floor Plan 2015
Grand Hyatt Shanghai
1.5m
1.5m
1.5m
1.5m
1.5m
19 18
17 16 15 14 13 12
23 24 25
27 28 2926
20
21
1 2
3 4 5 6
11
10
9
8
7
6.30m6.57m
Booked
Booked
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Reserved Reserved
Entrance
Entrance
22
Booked Booked Booked
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19-22 May 2015
GRAND HYATT SHANGHAI
CHINA
International Marketing Partner:
Media Partners:
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SPONSORSHIP & EXHIBITION
GOLD SPONSOR BRONZE SPONSORS
ASSOCIATE SPONSORS SESSION SPOTLIGHT SPONSORS
EXHIBITORS
Associations:
Why You Should Sponsor
Position your brand as the market leader in the biopharma industry
Stand out amidst competition
Showcase your latest technologies and solutions
Generate new business contacts
Strengthen existing relationships and partnerships in the industry
For more information about how you can leverage on our
events to optimize your marketing budget and reach your
target audience, please contact: Ms. Yvonne Leong at
Tel: +65 6508 2489 Email: Yvonne.leong@ibcasia.com.sg
8. 20 - 21 May 2015 • Tick the Main Conference of Interest
❑ 4th Cell Line Development & Engineering
❑ 6th Biosimilars Asia
❑ 5th Annual Biomanufacturing
19 & 22 May • Tick the Workshop(s) You Would Like to Attend
19 May • Pre-Conference 0.5 Day Workshops
❑ 9.00am - 12.30pm • Best Practices in Process Technology Transfer & cGMP
❑ 1.30pm - 5.00pm • Achieving Operational Excellence in Bioprocessing
19-May • Pre-Conference 1 Day Workshop
❑ 9.00am - 4.00pm • Monoclonal Antibodies
❑ 9.00am - 4.00pm • Boehringer Ingelheim Move to China (Incl. Site Tour)
22 May • Post-Conference 0.5 Day Workshops
❑ 9.00am - 12.30pm • Market Access Strategies for Biosimilars in Emerging Markets
❑ 1.30pm - 5.00pm • Gaining Approvals for Biosimilars in the US & Europe
22-May • Post-Conference 1 Day Workshops
❑ 9.00am - 4.00pm • Cutting Edge Trends in Antibody Development
❑ 9.00am - 4.00pm • Best CAPA & Root Cause Analysis Practices for Biomanufacturing
If undelivered, please return to:
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