This document announces an upcoming conference on pre-filled syringes to take place from April 5-7, 2011 in the USA. It highlights key speakers from pharmaceutical companies and regulatory agencies who will discuss technological advances, industry expectations, and developments in materials, processing, and regulatory issues regarding pre-filled syringes. Attendees will learn about the growing market for pre-filled syringes and have opportunities to network and participate in panel discussions. The conference aims to help attendees stay informed of latest trends in pre-filled syringe design, components, manufacturing, and quality.
This document summarizes an upcoming conference on pre-filled syringes in Europe. The two-day conference will feature presentations and discussions on pre-filled syringe formulations, filling and finishing processes, primary and secondary packaging developments, regulatory compliance, and patient safety approaches. It will also include two post-conference workshops on self-injection devices and safety issues within pre-filled syringes. Key industry leaders and experts will speak on topics such as biologics formulations, extractables and leachables, facility design strategies, and regulatory trends. The conference aims to explore challenges and solutions for pre-filled syringe development and commercialization.
This document provides information about an upcoming conference on 4th Pre-Filled Syringes that will address challenges in developing efficacious pre-filled syringe products. The conference will take place from October 17-19, 2011 in London and will feature key speakers from companies such as AstraZeneca, Novartis, Bayer, and the UK Medicines and Healthcare products Regulatory Agency (MHRA). It will include topics such as manufacturing, formulation, quality, safety, and novel pre-filled syringe technologies. Attendees can gain insights on issues like ensuring drug identity, potency and sterility in pre-filled syringes.
A syringe is essentially a device used in medicine to inject fluid into or withdraw fluid from the body. Medical syringes consist of a needle attached to a hollow cylinder that is fitted with a sliding plunger. The downward movement of the plunger injects fluid; upward movement withdraws fluid. A prefilled syringe is a single-dose packet of vaccine to which a needle has been fixed by the manufacturer. A prefilled syringe is not positioned as a high technology product such as needle free injectors which involves pioneering drug delivery technologies. Neither is it a simple technology (for example tabulating). Instead it is positioned in the middle, being on the border line of simple to advance.
The growth rate is to be expected to remain at a high level of more than 10% annually. This is due to a number of factors such as greater medication safety and increased convenience from using a prefillable device.
Prefilled syringes accommodate volumes that typically range from 0.25 to 5.0 ml. They are therefore best suited to products administered by subcutaneous or intramuscular injection. The categories account for the bulk of prefilled syringes: vaccines, blood stimulants, therapeutic proteins, erythroproteins, interferons and rheumatoid arthritis
Robert T. Fraley presents an overview of Monsanto's product pipeline and research process. The pipeline has 5 phases from early discovery through pre-commercial preparation. Projects are sorted into categories that provide benefits to farmers, processors, or consumers. Field trials are conducted in phases 2-4 to test product candidates before potential commercial launch in phase 5. The average duration and probability of success increases at each phase as products are further developed and evaluated.
The document discusses using a tobacco-based manufacturing platform for rapidly and cost-effectively producing vaccines and therapeutics. It outlines the business model, which involves licensing the technology to larger biotech companies, and describes initial customer feedback indicating the flu vaccine market may be difficult to enter but the therapeutics market, such as for alpha-1 antitrypsin, could be more promising. Prototyping efforts involve further characterizing alpha-1 antitrypsin production in tobacco plants.
This document provides an overview of biopharmaceutical manufacturing outsourcing to Asia. It discusses the complexities of biopharmaceutical production and why many companies outsource this work. It outlines key considerations for choosing a contract manufacturing organization (CMO) in Asia, including ensuring cGMP compliance, technical competence, intellectual property protection, and effective communication. The document briefly reviews the history of bioprocessing in Asia and provides examples of current CMOs in various Asian countries with relevant production capabilities.
This document provides information about the 4th Annual Biomarkers conference taking place on December 1-2, 2011 in London. The conference will cover biomarkers from discovery through clinical trials and safety. Key speakers will discuss regulatory perspectives, novel biomarker targets, how biomarkers can accelerate clinical development, and more. Attendees will learn about improvements in biomarker technologies and analyses of biomarkers' role in drug development. Poster presentations are encouraged. The global biomarkers market was estimated at $13.5 billion in 2010 and is predicted to reach $33.3 billion by 2015, driving growth in the industry.
UL Product Mindset Industry Report Household ChemicalsUL
The document summarizes key findings from a study on the household chemicals industry. It finds that:
1) Manufacturers are confident in their product safety and innovation but less so in sustainability. Rising costs are their biggest supply chain challenge.
2) Product reliability impacts manufacturers' ability to compete currently, while innovation will be most important in the future.
3) Manufacturers see themselves as responsible for product safety and communicating it to consumers.
4) Consumers find product safety and performance most important when evaluating household chemicals and have concerns about long term exposure and skin irritation.
5) It is difficult for consumers to find product safety information about household chemicals.
This document summarizes an upcoming conference on pre-filled syringes in Europe. The two-day conference will feature presentations and discussions on pre-filled syringe formulations, filling and finishing processes, primary and secondary packaging developments, regulatory compliance, and patient safety approaches. It will also include two post-conference workshops on self-injection devices and safety issues within pre-filled syringes. Key industry leaders and experts will speak on topics such as biologics formulations, extractables and leachables, facility design strategies, and regulatory trends. The conference aims to explore challenges and solutions for pre-filled syringe development and commercialization.
This document provides information about an upcoming conference on 4th Pre-Filled Syringes that will address challenges in developing efficacious pre-filled syringe products. The conference will take place from October 17-19, 2011 in London and will feature key speakers from companies such as AstraZeneca, Novartis, Bayer, and the UK Medicines and Healthcare products Regulatory Agency (MHRA). It will include topics such as manufacturing, formulation, quality, safety, and novel pre-filled syringe technologies. Attendees can gain insights on issues like ensuring drug identity, potency and sterility in pre-filled syringes.
A syringe is essentially a device used in medicine to inject fluid into or withdraw fluid from the body. Medical syringes consist of a needle attached to a hollow cylinder that is fitted with a sliding plunger. The downward movement of the plunger injects fluid; upward movement withdraws fluid. A prefilled syringe is a single-dose packet of vaccine to which a needle has been fixed by the manufacturer. A prefilled syringe is not positioned as a high technology product such as needle free injectors which involves pioneering drug delivery technologies. Neither is it a simple technology (for example tabulating). Instead it is positioned in the middle, being on the border line of simple to advance.
The growth rate is to be expected to remain at a high level of more than 10% annually. This is due to a number of factors such as greater medication safety and increased convenience from using a prefillable device.
Prefilled syringes accommodate volumes that typically range from 0.25 to 5.0 ml. They are therefore best suited to products administered by subcutaneous or intramuscular injection. The categories account for the bulk of prefilled syringes: vaccines, blood stimulants, therapeutic proteins, erythroproteins, interferons and rheumatoid arthritis
Robert T. Fraley presents an overview of Monsanto's product pipeline and research process. The pipeline has 5 phases from early discovery through pre-commercial preparation. Projects are sorted into categories that provide benefits to farmers, processors, or consumers. Field trials are conducted in phases 2-4 to test product candidates before potential commercial launch in phase 5. The average duration and probability of success increases at each phase as products are further developed and evaluated.
The document discusses using a tobacco-based manufacturing platform for rapidly and cost-effectively producing vaccines and therapeutics. It outlines the business model, which involves licensing the technology to larger biotech companies, and describes initial customer feedback indicating the flu vaccine market may be difficult to enter but the therapeutics market, such as for alpha-1 antitrypsin, could be more promising. Prototyping efforts involve further characterizing alpha-1 antitrypsin production in tobacco plants.
This document provides an overview of biopharmaceutical manufacturing outsourcing to Asia. It discusses the complexities of biopharmaceutical production and why many companies outsource this work. It outlines key considerations for choosing a contract manufacturing organization (CMO) in Asia, including ensuring cGMP compliance, technical competence, intellectual property protection, and effective communication. The document briefly reviews the history of bioprocessing in Asia and provides examples of current CMOs in various Asian countries with relevant production capabilities.
This document provides information about the 4th Annual Biomarkers conference taking place on December 1-2, 2011 in London. The conference will cover biomarkers from discovery through clinical trials and safety. Key speakers will discuss regulatory perspectives, novel biomarker targets, how biomarkers can accelerate clinical development, and more. Attendees will learn about improvements in biomarker technologies and analyses of biomarkers' role in drug development. Poster presentations are encouraged. The global biomarkers market was estimated at $13.5 billion in 2010 and is predicted to reach $33.3 billion by 2015, driving growth in the industry.
UL Product Mindset Industry Report Household ChemicalsUL
The document summarizes key findings from a study on the household chemicals industry. It finds that:
1) Manufacturers are confident in their product safety and innovation but less so in sustainability. Rising costs are their biggest supply chain challenge.
2) Product reliability impacts manufacturers' ability to compete currently, while innovation will be most important in the future.
3) Manufacturers see themselves as responsible for product safety and communicating it to consumers.
4) Consumers find product safety and performance most important when evaluating household chemicals and have concerns about long term exposure and skin irritation.
5) It is difficult for consumers to find product safety information about household chemicals.
Drug Delivery Systems Americas (2011) PpPiyush Patel
The two-day Drug Delivery Systems Americas conference in Boston will focus on the latest scientific research, manufacturing, and commercial opportunities in drug delivery systems. Key topics will include drug formulations for small molecules, proteins, peptides, and biologics; delivery technologies such as controlled release, nanotechnology, and biologics targeting; commercialization aspects including partnering, outsourcing, and regulations; and case studies. Over 20 industry leaders from companies including Novartis, Pfizer, Genzyme, and Abbott will present on challenges and innovations in developing advanced drug delivery technologies. Attendees will gain insights on enhancing bioavailability, managing product lifecycles, and identifying strategic partnerships in the growing field of drug delivery.
This document provides information about an upcoming conference on pre-filled syringes. It outlines the conference details including dates, location, key speakers from companies like Merck Serono and AstraZeneca. It also lists media partners, sponsors, and exhibitors. The document discusses the growing market for pre-filled syringes and challenges in the industry. It promotes the conference as a chance to learn about new developments, network, and address issues like drug compatibility and manufacturing processes. A pre-conference workshop on legal issues is also advertised.
2nd Pharmaceutical Anti Counterfeiting Americas (2011) PpPiyush Patel
This document provides information about the "2nd Pharmaceutical Anti-counterfeiting Americas" conference taking place on November 14-15, 2011 in Boston, USA. The conference will discuss combating counterfeit medicines and feature speakers from pharmaceutical companies and regulatory agencies. Attendees will learn about US policy updates, technologies for tracking pharmaceuticals, and best practices for supply chain integrity. Posters can be submitted by academic institutions, pharmaceutical companies, and service providers to share research results. The conference is aimed at professionals working in pharmaceutical supply chain security, anti-counterfeiting, brand protection, and related fields.
SMi's Pre-Filled Syringes Asia Pacific conference provides a fundamental analysis of the key growth drivers in the Asia-Pacific pre-filled syringes market. The conference brings together industry leaders to focus on opportunities and barriers to creating successful strategies in this emerging market. Register by March 31st to receive a $300 discount, or by April 28th to receive a $100 discount. The conference will take place on July 20-21, 2011 in Singapore and will include presentations and discussions on topics such as commercial opportunities, manufacturing, packaging, quality control, and regulatory trends related to pre-filled syringes in Asia-Pacific.
This document provides information about an upcoming conference on single-use bioreactors being held in London on November 1-2, 2012. The conference will feature speakers from pharmaceutical and biotech companies as well as equipment suppliers discussing topics such as using single-use bioreactors to increase flexibility, reduce costs and speed up research and development. Attendees will learn about case studies on scaling up production with disposable technology and accelerating cell culture development. The conference offers sponsorship and exhibition opportunities for companies to promote their services and products.
This investor presentation provides an overview of Viropro, Inc., a contract development and manufacturing organization for biotech drugs. It discusses the growing market opportunity in outsourcing biopharmaceutical R&D and manufacturing services. Viropro plans to build a global network through acquisitions like Alpha Biologics, which owns an FDA-compliant biomanufacturing facility in Malaysia. This "string of pearls" model across Asia and Europe is aimed to provide world-class development and manufacturing services to biotech companies in a cost-effective manner. The presentation makes the case that an investment of $40 million in Viropro over two funding rounds could yield a return of 10x and 46% IRR through an
This document provides an agenda for the "Aesthetics and Anti-Ageing" conference taking place on May 11-12, 2011 in London, UK. The conference will explore new developments in anti-aging therapies and latest technological advancements in aesthetic surgeries. Over the two days, keynote speakers will discuss topics such as changing market demands, innovations in facial rejuvenation surgeries, cosmeceuticals, fat stem cells, new technologies for delivering anti-aging agents to the skin, challenging surgical problems, platelet rich plasma, sports medicine, and more. The event is aimed at professionals in fields like pharmaceuticals, biotechnology, dermatology, anti-aging medicine, and aesthetic medicine.
This document announces the 5th Annual Stability Testing Conference to be held November 3-4, 2011 in London. The conference will bring together experts from pharmaceutical companies like Pfizer, GSK, Novartis, and others to discuss multiple facets of stability testing. Topics will include updates on guidelines, effective planning, methods, evaluation of results, challenges in biologics stability testing, and analytical testing methods.
This document provides information about the 7th Annual Pharmacovigilance conference to be held on January 30-31, 2012 in London. The conference will discuss current pharmacovigilance regulations and strategies to improve drug safety, with key speakers from major pharmaceutical companies. Topics will include pharmacovigilance throughout a drug's lifecycle, risk management, safety surveillance, and new EU regulations. Attendees will gain insights on evaluating safety signals and benefit-risk assessments to increase drug safety.
The document announces the 5th Annual Contract Manufacturing conference to take place on December 7-8, 2011 in London. It will address every aspect of outsourcing from selecting partners to regulatory issues. Key speakers include outsourcing managers from major pharmaceutical companies. Attendees will learn about emerging trends, selection criteria, partnership strategies, and regulatory frameworks. The conference aims to help pharmaceutical companies and contract manufacturers assess outsourcing strategies and opportunities.
Clinical Trial Logistics & Supply (2011) FbFateja
This document provides information about an upcoming clinical trial logistics and supply conference to be held in London on September 29-30, 2011. It lists key speakers from various pharmaceutical companies that will discuss topics like predictive drug supply modelling, bioequivalence studies, drug pooling strategies, quality assurance, and managing clinical trials in Eastern Europe. The document also provides details about sponsoring, exhibiting, and submitting poster presentations at the conference.
This document announces the 11th Annual Biosimilars UK conference taking place October 29-31, 2012 in London. It will bring together major pharmaceutical companies, regulatory bodies, CROs, CMOs, and law firms to discuss strategies for competing in the complex biosimilars market. Key topics will include the latest regulatory guidelines, financial viability, patent strategies, approval pathways, legal issues, preclinical/clinical challenges, the roles of the US and European markets, pricing/reimbursement, and pharmacovigilance. The goal is to help participants maximize opportunities in this changing landscape. Major sponsors include Merck Millipore and United BioSource Corporation.
This document provides information about an upcoming biobanking conference to take place on March 10-11, 2011 in London. It lists key speakers from companies like AstraZeneca, Bayer, and Sanofi-Aventis who will discuss topics like sample storage, biomarker discovery, and stem cell banking. The document also notes the growing market for biobanking and its importance for medical research. Sponsoring companies and media partners promoting the conference are also listed.
This document provides information about the 6th Annual Pharmacovigilance Conference taking place on March 16-17, 2011 in London. The conference will discuss the latest developments in pharmacovigilance, drug safety, and risk management. It will feature keynote speakers from organizations like Pfizer, Abbott Laboratories, and Novartis. Sessions over the two days will cover topics like benefit-risk assessments, signal detection methodologies, pharmacovigilance during clinical trials, and the transition between pre- and post-marketing safety. The conference is aimed at professionals in fields like pharmacovigilance, drug development, clinical safety, and regulatory affairs.
This document provides information about the 5th Lyophilisation conference to be held from September 7-9, 2011 in London. The conference will address key issues in lyophilisation process development and optimization. It will feature speakers from major pharmaceutical companies and contract manufacturing organizations. Attendees will learn about formulation characteristics, analytical technologies, process development, and engineering trends related to freeze-drying of pharmaceuticals and biologics. The conference is organized by Visiongain and will include workshops, presentations, panel discussions and opportunities for networking, exhibition and poster presentations.
The document provides information about the 5th Annual Recombinant Antibodies conference taking place from January 17-19, 2012 in London. It will feature presentations and workshops on advances in bispecific antibodies, next-generation monoclonal antibodies, and antibody translation. Key speakers will represent companies such as Roche, Novartis, MedImmune. Workshop topics will include antibody drug conjugates. The conference aims to provide networking opportunities and insights into improving antibody potency, engineering, development, and applications for cancer, inflammatory diseases, and more.
This document provides information about the "Pre-Filled Syringes Americas" conference taking place from March 31 - April 2, 2014 in Iselin, New Jersey. The conference will focus on the development, manufacture, and regulation of pre-filled syringe and injector devices in the Americas region. It will include presentations and panels from industry experts, as well as an exhibition and networking opportunities. Attendees will learn about topics like developing delivery systems for biologics, managing extractables and leachables, and gaining FDA approval. A half-day post-conference workshop on April 2nd will provide insight on accelerating regulatory approval of combination products.
The document is an invitation to the "Anti-Counterfeiting Americas" conference on November 8-9, 2010 in Boston. The conference will provide insights into issues related to securing the pharmaceutical supply chain and tracking technologies. Key topics will include tackling counterfeit drugs, improving distribution integrity, and collaboration against counterfeiting. Attendees will gain an understanding of supply chain challenges and investment potential in pharmaceutical logistics. The conference will feature speakers from organizations focused on supply chain security and counterfeit drug prevention.
This document provides information about the "Vaccine Research & Innovation 2010" conference taking place on September 2-3, 2010 in London. The conference will explore opportunities in vaccine research and development and feature key speakers from companies such as Novartis Vaccines, Merck, and Intercell. Attendees will gain insights into topics like overcoming challenges in cancer vaccine development, evaluating immune responses to combination vaccines, and implementing strategies for manufacturing conjugate vaccines. The conference is designed to share successful strategies and innovative technologies for developing more effective vaccines.
The document advertises the 8th annual Pre-Filled Syringes Americas conference and exhibition taking place from March 31st to April 2nd, 2014 in Iselin, New Jersey. The conference will bring together over 85 key decision makers from leading biotechnology and pharmaceutical companies to discuss developments in pre-filled syringes and injection devices over the course of two days of presentations, panel discussions, and workshops. Attendees will have the opportunity to network with industry leaders, evaluate solutions from exhibitors, and return to their businesses with the information and contacts needed to make decisions for their products.
The document summarizes the 3rd Annual Vaccine Manufacturing conference to be held in London on April 18-19, 2011. The conference will feature key speakers from major vaccine companies like Pfizer, Novartis, and MedImmune who will discuss strategies for better vaccine manufacturing and development. Attendees will learn about innovative technologies and strategies to address challenges in vaccine development and manufacturing. The conference will provide opportunities to identify new vaccine developments, review regulatory requirements, and explore business partnerships.
The document summarizes an upcoming conference on biobanking in the Americas from June 7-9, 2011 in Boston. It will bring together experts from biobanks, pharmaceutical companies, biotech firms, and regulatory agencies to discuss strategic approaches to biosample management and using biobanks to enable next-generation drug discovery and personalized medicine. Speakers will provide practical knowledge on new biobanking models, address ethical and legal challenges, and explore how to leverage biospecimen resources to support biomarker research. Attendees will learn best practices for biorepository management and implementation, applications of genome sequencing, and strategies for building biomarker discovery pipelines. The conference aims to facilitate networking and enable confident decision making through benchmarking against
Drug Delivery Systems Americas (2011) PpPiyush Patel
The two-day Drug Delivery Systems Americas conference in Boston will focus on the latest scientific research, manufacturing, and commercial opportunities in drug delivery systems. Key topics will include drug formulations for small molecules, proteins, peptides, and biologics; delivery technologies such as controlled release, nanotechnology, and biologics targeting; commercialization aspects including partnering, outsourcing, and regulations; and case studies. Over 20 industry leaders from companies including Novartis, Pfizer, Genzyme, and Abbott will present on challenges and innovations in developing advanced drug delivery technologies. Attendees will gain insights on enhancing bioavailability, managing product lifecycles, and identifying strategic partnerships in the growing field of drug delivery.
This document provides information about an upcoming conference on pre-filled syringes. It outlines the conference details including dates, location, key speakers from companies like Merck Serono and AstraZeneca. It also lists media partners, sponsors, and exhibitors. The document discusses the growing market for pre-filled syringes and challenges in the industry. It promotes the conference as a chance to learn about new developments, network, and address issues like drug compatibility and manufacturing processes. A pre-conference workshop on legal issues is also advertised.
2nd Pharmaceutical Anti Counterfeiting Americas (2011) PpPiyush Patel
This document provides information about the "2nd Pharmaceutical Anti-counterfeiting Americas" conference taking place on November 14-15, 2011 in Boston, USA. The conference will discuss combating counterfeit medicines and feature speakers from pharmaceutical companies and regulatory agencies. Attendees will learn about US policy updates, technologies for tracking pharmaceuticals, and best practices for supply chain integrity. Posters can be submitted by academic institutions, pharmaceutical companies, and service providers to share research results. The conference is aimed at professionals working in pharmaceutical supply chain security, anti-counterfeiting, brand protection, and related fields.
SMi's Pre-Filled Syringes Asia Pacific conference provides a fundamental analysis of the key growth drivers in the Asia-Pacific pre-filled syringes market. The conference brings together industry leaders to focus on opportunities and barriers to creating successful strategies in this emerging market. Register by March 31st to receive a $300 discount, or by April 28th to receive a $100 discount. The conference will take place on July 20-21, 2011 in Singapore and will include presentations and discussions on topics such as commercial opportunities, manufacturing, packaging, quality control, and regulatory trends related to pre-filled syringes in Asia-Pacific.
This document provides information about an upcoming conference on single-use bioreactors being held in London on November 1-2, 2012. The conference will feature speakers from pharmaceutical and biotech companies as well as equipment suppliers discussing topics such as using single-use bioreactors to increase flexibility, reduce costs and speed up research and development. Attendees will learn about case studies on scaling up production with disposable technology and accelerating cell culture development. The conference offers sponsorship and exhibition opportunities for companies to promote their services and products.
This investor presentation provides an overview of Viropro, Inc., a contract development and manufacturing organization for biotech drugs. It discusses the growing market opportunity in outsourcing biopharmaceutical R&D and manufacturing services. Viropro plans to build a global network through acquisitions like Alpha Biologics, which owns an FDA-compliant biomanufacturing facility in Malaysia. This "string of pearls" model across Asia and Europe is aimed to provide world-class development and manufacturing services to biotech companies in a cost-effective manner. The presentation makes the case that an investment of $40 million in Viropro over two funding rounds could yield a return of 10x and 46% IRR through an
This document provides an agenda for the "Aesthetics and Anti-Ageing" conference taking place on May 11-12, 2011 in London, UK. The conference will explore new developments in anti-aging therapies and latest technological advancements in aesthetic surgeries. Over the two days, keynote speakers will discuss topics such as changing market demands, innovations in facial rejuvenation surgeries, cosmeceuticals, fat stem cells, new technologies for delivering anti-aging agents to the skin, challenging surgical problems, platelet rich plasma, sports medicine, and more. The event is aimed at professionals in fields like pharmaceuticals, biotechnology, dermatology, anti-aging medicine, and aesthetic medicine.
This document announces the 5th Annual Stability Testing Conference to be held November 3-4, 2011 in London. The conference will bring together experts from pharmaceutical companies like Pfizer, GSK, Novartis, and others to discuss multiple facets of stability testing. Topics will include updates on guidelines, effective planning, methods, evaluation of results, challenges in biologics stability testing, and analytical testing methods.
This document provides information about the 7th Annual Pharmacovigilance conference to be held on January 30-31, 2012 in London. The conference will discuss current pharmacovigilance regulations and strategies to improve drug safety, with key speakers from major pharmaceutical companies. Topics will include pharmacovigilance throughout a drug's lifecycle, risk management, safety surveillance, and new EU regulations. Attendees will gain insights on evaluating safety signals and benefit-risk assessments to increase drug safety.
The document announces the 5th Annual Contract Manufacturing conference to take place on December 7-8, 2011 in London. It will address every aspect of outsourcing from selecting partners to regulatory issues. Key speakers include outsourcing managers from major pharmaceutical companies. Attendees will learn about emerging trends, selection criteria, partnership strategies, and regulatory frameworks. The conference aims to help pharmaceutical companies and contract manufacturers assess outsourcing strategies and opportunities.
Clinical Trial Logistics & Supply (2011) FbFateja
This document provides information about an upcoming clinical trial logistics and supply conference to be held in London on September 29-30, 2011. It lists key speakers from various pharmaceutical companies that will discuss topics like predictive drug supply modelling, bioequivalence studies, drug pooling strategies, quality assurance, and managing clinical trials in Eastern Europe. The document also provides details about sponsoring, exhibiting, and submitting poster presentations at the conference.
This document announces the 11th Annual Biosimilars UK conference taking place October 29-31, 2012 in London. It will bring together major pharmaceutical companies, regulatory bodies, CROs, CMOs, and law firms to discuss strategies for competing in the complex biosimilars market. Key topics will include the latest regulatory guidelines, financial viability, patent strategies, approval pathways, legal issues, preclinical/clinical challenges, the roles of the US and European markets, pricing/reimbursement, and pharmacovigilance. The goal is to help participants maximize opportunities in this changing landscape. Major sponsors include Merck Millipore and United BioSource Corporation.
This document provides information about an upcoming biobanking conference to take place on March 10-11, 2011 in London. It lists key speakers from companies like AstraZeneca, Bayer, and Sanofi-Aventis who will discuss topics like sample storage, biomarker discovery, and stem cell banking. The document also notes the growing market for biobanking and its importance for medical research. Sponsoring companies and media partners promoting the conference are also listed.
This document provides information about the 6th Annual Pharmacovigilance Conference taking place on March 16-17, 2011 in London. The conference will discuss the latest developments in pharmacovigilance, drug safety, and risk management. It will feature keynote speakers from organizations like Pfizer, Abbott Laboratories, and Novartis. Sessions over the two days will cover topics like benefit-risk assessments, signal detection methodologies, pharmacovigilance during clinical trials, and the transition between pre- and post-marketing safety. The conference is aimed at professionals in fields like pharmacovigilance, drug development, clinical safety, and regulatory affairs.
This document provides information about the 5th Lyophilisation conference to be held from September 7-9, 2011 in London. The conference will address key issues in lyophilisation process development and optimization. It will feature speakers from major pharmaceutical companies and contract manufacturing organizations. Attendees will learn about formulation characteristics, analytical technologies, process development, and engineering trends related to freeze-drying of pharmaceuticals and biologics. The conference is organized by Visiongain and will include workshops, presentations, panel discussions and opportunities for networking, exhibition and poster presentations.
The document provides information about the 5th Annual Recombinant Antibodies conference taking place from January 17-19, 2012 in London. It will feature presentations and workshops on advances in bispecific antibodies, next-generation monoclonal antibodies, and antibody translation. Key speakers will represent companies such as Roche, Novartis, MedImmune. Workshop topics will include antibody drug conjugates. The conference aims to provide networking opportunities and insights into improving antibody potency, engineering, development, and applications for cancer, inflammatory diseases, and more.
This document provides information about the "Pre-Filled Syringes Americas" conference taking place from March 31 - April 2, 2014 in Iselin, New Jersey. The conference will focus on the development, manufacture, and regulation of pre-filled syringe and injector devices in the Americas region. It will include presentations and panels from industry experts, as well as an exhibition and networking opportunities. Attendees will learn about topics like developing delivery systems for biologics, managing extractables and leachables, and gaining FDA approval. A half-day post-conference workshop on April 2nd will provide insight on accelerating regulatory approval of combination products.
The document is an invitation to the "Anti-Counterfeiting Americas" conference on November 8-9, 2010 in Boston. The conference will provide insights into issues related to securing the pharmaceutical supply chain and tracking technologies. Key topics will include tackling counterfeit drugs, improving distribution integrity, and collaboration against counterfeiting. Attendees will gain an understanding of supply chain challenges and investment potential in pharmaceutical logistics. The conference will feature speakers from organizations focused on supply chain security and counterfeit drug prevention.
This document provides information about the "Vaccine Research & Innovation 2010" conference taking place on September 2-3, 2010 in London. The conference will explore opportunities in vaccine research and development and feature key speakers from companies such as Novartis Vaccines, Merck, and Intercell. Attendees will gain insights into topics like overcoming challenges in cancer vaccine development, evaluating immune responses to combination vaccines, and implementing strategies for manufacturing conjugate vaccines. The conference is designed to share successful strategies and innovative technologies for developing more effective vaccines.
The document advertises the 8th annual Pre-Filled Syringes Americas conference and exhibition taking place from March 31st to April 2nd, 2014 in Iselin, New Jersey. The conference will bring together over 85 key decision makers from leading biotechnology and pharmaceutical companies to discuss developments in pre-filled syringes and injection devices over the course of two days of presentations, panel discussions, and workshops. Attendees will have the opportunity to network with industry leaders, evaluate solutions from exhibitors, and return to their businesses with the information and contacts needed to make decisions for their products.
Similar to 2nd prefilled syringes americas (2011) (20)
The document summarizes the 3rd Annual Vaccine Manufacturing conference to be held in London on April 18-19, 2011. The conference will feature key speakers from major vaccine companies like Pfizer, Novartis, and MedImmune who will discuss strategies for better vaccine manufacturing and development. Attendees will learn about innovative technologies and strategies to address challenges in vaccine development and manufacturing. The conference will provide opportunities to identify new vaccine developments, review regulatory requirements, and explore business partnerships.
The document summarizes an upcoming conference on biobanking in the Americas from June 7-9, 2011 in Boston. It will bring together experts from biobanks, pharmaceutical companies, biotech firms, and regulatory agencies to discuss strategic approaches to biosample management and using biobanks to enable next-generation drug discovery and personalized medicine. Speakers will provide practical knowledge on new biobanking models, address ethical and legal challenges, and explore how to leverage biospecimen resources to support biomarker research. Attendees will learn best practices for biorepository management and implementation, applications of genome sequencing, and strategies for building biomarker discovery pipelines. The conference aims to facilitate networking and enable confident decision making through benchmarking against
The document announces the 7th Annual Monoclonal Antibody conference to be held from May 18-20th, 2011 in London. It will examine new therapeutic applications and technological developments of monoclonal antibodies. Key speakers from companies like Abbott, Pfizer, Bristol-Myers Squibb, and Novartis will discuss topics like preclinical safety evaluation, therapeutic targets for diseases, advances in antibody technology, production techniques, and trends in capacity utilization. Attendees will learn about monoclonal antibody discovery, development, and regulatory issues.
This document provides an agenda for the "2nd Prefilled Syringes Americas" conference taking place from April 5-7, 2011 in the USA. The conference will discuss trends in pre-filled syringes including new materials, components, and processes. Key topics include plastic syringe systems, drug delivery devices, technological developments, and advanced formulations for biologics. Speakers will represent companies like Bristol-Myers Squibb, Gerresheimer, West Pharmaceutical, and Arecor. The event aims to explore industry requirements and the latest innovations in pre-filled syringe product development.
2nd annual diabetes and diabetic retinopathy (2011)Pranita Nangia
This document announces the 2nd Annual Diabetes and Diabetic Retinopathy conference to be held on June 15-16, 2011 in London. The conference will bring together industry experts to discuss drug development for diabetes and diabetic retinopathy. Key topics will include current and emerging treatments for diabetes and retinal diseases, challenges in developing novel therapies, and clinical trials. Media partners for the event include PharmiWeb.com, Biotechnology Europe, Future Pharmaceuticals, and InPharm.
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Reasons to register today:
• Understand the use of isothermal calorimetry to characterise stability of amorphous pharmaceuticals
• Implement the latest technological developments
• Discuss the best approaches to control and stabilise amorphous drug forms
• Examine the quantification of amorphous content
• Gain a clearer insight on amorphous food materials
• Seize this opportunity to network with leaders from pharma-biotech, healthcare and regulatory agencies
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2nd prefilled syringes americas (2011)
1. CALL
NOW FOR
EARLY BIRD
2nd Prefilled
DISCOUNTS
Syringes Americas
Examining the current market demand and developing safer, stable, cost-effective pre-filled syringes
April 5th - 7th 2011, USA BOOK NOW!
Key Speakers
Dr.Ingrid Markovic,Expert Review Scientist , Food and Drug Administration
Pankaj Paranjpe, Manager, R&D Operations, Bristol-Myers Squibb
Jennifer Johns, Principal Packaging Engineer, Bristol-Myers Squibb
Amanda Wolf, Scientist - Pharmaceutical Research and Development, Pfizer
Crisanta Ransom, MS&T - Commercialization Technical Center, Eli Lilly
Raul Soikes, Sr. Director Program Management, Baxter BioPharma Solutions
Dr. Jan Jezek, Chief Scientific Officer, Arecor
Jim Spolyar, Sales and Technical Director, SKAN US
Stephen A. Barat, Director, Toxicology and Operations, Forest Research Institute
Vinod Vilivalam, Director, West Pharmaceutical
Dr. Arno Fries Director Product Management Tubular Glass, Gerresheimer Bünde
Dr.Silke Conrad, Manager Regulatory Affairs, Ypsomed AG
Patty Kiang, Consultant, Kiang Consultant Services
Pre-conference Workshop, Tuesday April 5th 2011
Develop syringe materials and components that minimize and eliminate: contamination from leachables and extractables
Led by: Dr. Patty Kiang, PhD, Consultant, Kiang Consultant Services
Associate Sponsor
Organised By
Driving the Industry Forward | www.futurepharmaus.com
Media Partners
To Book Call: +44 (0) 20 7336 6100 | www.visiongain.com/pfsamericas
2. Conference Introduction
2nd Prefilled Syringes Americas
April 5th - 7th 2011, USA
Dear Colleague,
ontinuous growth in vaccines, blood stimulants, therapeutic proteins,
C Poster Presentation
erythroproteins, interferons and rheumatoid arthritis has driven the growth of pre-
filled syringes market At a busy conference it is hard to make sure everyone who
ith promising growth of 10-15% per annum, there were 2 billion pre-filled syringe
W shares your interests knows what you are doing. Maximise
units sold in 2009 alone and expected to continue reaching 3.64bn units in 2015 your time at Visiongain’s 2nd Prefilled syringes Americas
and 6.83bn by 20251.
meeting by sharing your results in a poster presentation.
afety, stability, convenience and cost-effectiveness are main factors driving growth
S
With a plethora of key decision makers, take advantage of
of the pre-filled syringes market. Prefilled syringe manufacturers have had to
therefore respond to increasing demand, new requirements and more sophisticated this senior networking opportunity.
forms of drug delivery.
Please send your 200 word abstract, in English, to:
ollowing the success of visiongain’s previous pre-filled syringes conferences, we are
F info@visiongainglobal.com for approval. The deadline
proud to present the 2nd Pre-filled Syringes Americas conference.
for submissions is Monday, March 21st, 2011. Please include
t this global event of pre-filled syringes, meet industry leaders from around the
A
contact details for the corresponding author(s).
world to discuss every aspect of pre-filled syringes market from technological
needs, design to safety and quality through to regulatory issues. Spend three days in Academic institutions will not be charged a fee if booked as
partnering; participate in special panel discussions and evening networking drinks.
full-price delegates. Posters submitted by pharmaceutical
tay ahead of competition by learning about the latest developments on
S
and biotechnology firms will be charged a fee of £199.
technological advances in design, component materials, process engineering,
siliconisation, dosage accuracy, auto-injections, quality, safety and regulatory issues. Posters submitted by service providers / vendors are
welcome and will be subject to evaluation. Upon
By attending this conference, you will:
approval a fee of £500 will apply. Two delegates from
• ear about new technological developments and changing market scenario
H
your organisation must be booked at full price to present
• nderstand pharmaceutical industry expectations from manufacturers of pre-
U
a poster.
fillable syringes
• earn about recent achievements and trends for formulation and delivery of
L Please note that all posters will be displayed at the
protein pharmaceuticals, vaccines and blood stimulant drugs discretion of Visiongain Ltd and are subject to approval.
• ain insight about developments in the areas of component materials, surface
G Due to limited space, please register your interest early.
treatments and filling processing and packaging
• vercome challenges in prefilled syringes design, liquid viscosity, injection speed/
O
flow rate, needle inner diameter, needle length etc
• xplore auto-injection devices: convenience items, or a key component of
E Who will attend?
injectable products
• ptimize siliconization with regard to product requirements, autoinjector
O Vice/Presidents, Directors, Heads of:
compatibility, general syringe performance
• Packaging
• iscover about applications & advantages of bubble-free filling for today’s
D
parenteral products • Labelling
• evelop syringe materials and components that minimize and eliminate:
D
contamination from leachables and extractables
• Manufacturing
• tay ahead by learning about Ingenious advanced labelling technologies, including
S • Product design
peel off tabs and radio frequency transmitters, to increase product safety and
security • Technical support
• eview current state of art and future technological developments in the field of
R • Drug product process development
RABS, isolators, e-beam and alternatives
• xamine factors and recent developments in processing syringe nests
E • Drug device process development
• valuate benefits and challenges of outsourcing
E • Pharmaceutical sciences
• ssess the impact of new post-market surveillance regulations on pre-filled
A
medical devices • Safe medication practice
• btain the latest market analysis, and meet manufacturers showcasing their
O • Drug discovery & delivery
leading products
• Strategic alliances
I look forward to meeting you at the conference
• Clinical product resourcing
Best regards
• Supply outsourcing
• Contract management
• Process development
Sonia Tomar • Investment and venture capital
Conference Producer
1
Pre-Filled Syringes and Related Systems: World Market Outlook 2010-2025
3. Pre-Conference Interactive Workshop
2nd Prefilled Syringes Americas
Tuesday April 5th 2011
Develop syringe materials and components that minimize and
eliminate: contamination from leachables and extractables
Led by: Dr. Patty Kiang Timings: 9:30 - 10:00 Coffee & Registration
0
Consultant 10:00 - 17:00 Workshop
Kiang Consultant Services T
iming includes lunch and refreshment breaks
Workshop Agenda: About your workshop leader:
The objective of this workshop is to provide the information Dr. Patty Kiang
of critical factors which will impact the success of the prefilled Patty H Kiang, Ph.D. is a Pharmaceutical Consultant on
syringe development. The material composition, component / Pharmaceutical packaging and delivery devices for liquid and
lyophilized products, Prefilled syringe system, and CMC filing
device design, manufacturing and sterilization processes are
for Combination Products.
all the important factors which will impact the extractables
Prior to the consultant position, she was Account Director for Catalent Pharma
and leachables from the syringe system. Improved glass syringe Solutions; she was responsible for business development of Analytical & Biotech
operation and COC resin or Daikyo CZ resin syringes plus Services to Biotech and Pharmaceutical companies on the West Coast of USA,
Canada and Asia pacific territory.
Fluorocarbon film laminated plungers have demonstrated the
She was Head of Device Development for Genentech Inc. in South San Francisco,
reduction of contamination from extractables and leachables will
CA. She was responsible for the development of a new autopen injector for
be discussed in the workshop Growth Hormone; she was also responsible for setting up the Extractable /
Leachable program for evaluation of primary container/closure systems and
was a CMC leader for a prefilled syringe drug development. Prior to joining
Genentech, she was Director, Delivery Device and Packaging Support for
N
EW
Schering Plough, in Kenilworth, NJ. She was responsible for the development
RE
Pre-Filled Syringes and Related Systems: of PEG-Interferon dual chamber pen injector and various delivery devices. Prior
PO
World Market Outlook 2010-2025
RT
to joining Schering Plough, she was Director of Technology Development for
– how will rising demand and technological West Pharmaceutical Services in Lionville, PA, a developer and manufacturer of
developments create opportunities?
parental drug packaging components, where she coordinated with corporate
The market for pre-filled syringes has achieved growth partners in Japan and Germany in the development of various new products.
in recent years. In 2009, an estimated 2 billion pre-
filled syringe units were sold and the market for that She was a member of the faculty of the PDA’s Training and Research Institute,
technology was estimated to be worth up to $2.5 where she taught courses on Parenteral Packaging, and served as a member
billion. There is a trend towards pre-filled drug injection
of USP’s Expert Committee on Drug Packaging, Storage and Distribution. She
systems, away from vials/ampules, for both new and
existing products. Examples are filled glass and plastic was the chairperson for PDA Gamma Radiation Sterilization of Polymeric
syringes, pens and low-volume auto-injection devices, Materials Committee. She is an expert in the area of drug and container/closure
including refills. That sector has shown growth of
interactions and compability issues.
10-15% in recent years, forming one of the fastest-
expanding sectors in the pharmaceutical industry. In our She is a frequent speaker and has chaired many symposia on the packaging of
new report, we predict that the pre-filled drug delivery pharmaceutical and biotechnology derived products. Most recently she chaired
market will grow steadily from 2010, as the number
of products launched in pre-filled injectable forms the PDA 2006 Global Prefilled Syringe & Injection Device Conference. Dr. Kiang
increases. Medical professionals, patients and other holds five patents in the field of polymeric surface coatings. She received a Ph.D. in
stakeholders see the benefits of that more-convenient Analytical Chemistry from Villanova University and holds an MBA from Pennsylvania
system, raising demand at the expense of older formats.
State University.
4. Day 1
2nd Prefilled Syringes Americas
Wednesday April 6th 2011
09:00 Registration and refreshments 12:40 Networking lunch
09:30 Opening address from the chair 13:40 Overview of drug delivery devices for pre-filled
Pankaj Paranjpe syringe products
Bristol-Myers Squibb • User Benefit
• A new generation of device and compromises in device design
Jennifer Johns
• Aseptic pre-filled drug-delivery systems
Bristol-Myers Squibb
• Future opportunities
09:40 Update on pre-filled syringes: trends, materials,
14:20 Sponsor Spotlight Session
components, processes and quality
T
ake this unique opportunity to be a part of the conference theme,
• Market dynamics and trends
network, share ideas and provide an overview of your product/services
• New syringe materials
to the audience.
• Value added components
For more information please contact ronald.magali@visiongainglobal.com
• Syringes for biotech drugs
• Quality aspects
Dr. Arno Fries
15:00 Afternoon Refreshments
Director Product Management Tubular Glass
Gerresheimer
15:20 Panel discussion: New technological developments
and changing market scenario
10:20 Recent trends in the application of plastic prefillable
P
anlists will discuss the market trends and emerging requirements, latest
syringe systems for biopharmaceutical drug delivery developments in all areas of pre-filled syringe product development; from
• yclic olefin polymers: properties, applications and commercial drug products
C formulation to manufacturing, considerations for component and system
• ecent trends in the use of newer plastics for delivering mAbs,
R selection, supplier role in quality for any questions or participation please
proteins and vaccines contact sonia.tomar@visiongainglobal.com
• olve challenges associated with glass prefilled syringes, including
S
breakage reactivity and leachables like silicone, tungsten and glue
• arket and scientific needs for plastic prefillable syringes for
M
biopharmaceutical drugs and high viscosity formulations 16:00 Advanced formulations of biologics
• lastic vials for break resistant, less reactive and cold temperature
P • Stability of biologics
storage/transport containers for biologics and stem cells • Stable aqueous formulations for pre-filled syringes
• Reduced rate of aggregation
Vinod Vilivalam • High concentrations of antibodies
Director • Terminal sterilization by gamma radiation or e-beam
West Pharmaceutical
Dr. Jan Jezek
Chief Scientific Officer
Arecor Limited
11:00 Morning refreshments
16:40 Closing remarks from the chair
11:20 Rational selection of primary packaging components
for pre-filled syringe products
• Primary packaging components
• Packaging and drug delivery trends 16:50 Networking Drinks
• Developing primary and critical secondary packaging components Take your discussions further and build new
relationships in a relaxed and informal setting.
12:00 Fill-finish for prefilled syringes in a contract
manufacturing setting with the following emphasis
N
EW
• lient Teams dedicated to your product – relentless focus on your product
C Pharma Business Daily
SL
by knowledgeable individuals
ET
Each issue of Pharma Business Daily newsletter focuses on latest
• etrics to drive performance – leading indicating metrics; tangible output
M
TE
breaking stories in your market. Delivered directly to your Inbox or
R
translating to a timely deliverable available through the website, all the industry news is available to you
• CMO-Client partnership – conclusion highlighting best practices all the time. When you want the news its there for you - it really is that
simple. Over 25+ stories everyday as they happen. Never again will any
Raul Soikes of your colleagues be aware of news that you aren’t.
Sr. Director Program Management Plus exclusive features from visiongain conferences and in-depth
Baxter BioPharma Solutions analysis from visiongain analysts will be available to you thanks to your
subscription to PharmaBusinessDaily. This information is not available
anywhere else.
Call +44 (0)207 336 6100 or visit www.visiongain.com to sign up.
Due to unforeseen circumstances the programme may change and visiongain reserves the right to alter the venue and/or speakers c Copyright visiongain Ltd, 2011
5. Day 2
2nd Prefilled Syringes Americas
Thursday April 7th 2011
09:00 Registration and refreshments 13:40 Pre-filled syringe processing with RABS, Isolators,
E-beam & Alternatives
• Isolator technology with latest E-Beam design features
09:30 Opening address from the chair • Comparison of RABS vs Isolators
• Alternative tub entry system for slow speed production
• Expansion of the areas of application of syringe technology
Jim Spolyar
09:40 Extractables and leachables in pre-filled syringes
Sales and Technical Director
Dr. Ingrid Markovic SKAN US
Expert Review Scientist
Food and Drug Administration
14:20 Processing solutions for pre-filled syringes from
conditioning to aseptic filling and final assembly
10:20 How to select syringe components - Minimize • yringe conditioning including the processing steps washing, silicone
S
potential extractables and leachables coating, needle or needle shield assembly, nesting and packaging
• Tips to establish user requirements - Special topic: Features and challenges of the silicone coating process
• Examples of extractable/leachable failure modes experienced by industry • n-line washing and sterilizing solutions (for syringes without a glued-in needle)
I
• Risk based approach in evaluating extractables/leachables - pecial topic: Sterilizing tunnel for syringes with non-glass-to-glass
S
• trategy for selecting syringe components used for different drug products
S contact transport system
and coming from various sources • septic filling including the processing steps debagging, delidding, filling
A
and closing
Crisanta Ransom, Ph.D. - pecial topic: Vacuum filling and closing as well as in-process control
S
MS&T - Commercialization Technical Center (IPC) capabilities
Eli Lilly and Company • ssembly including the processing steps denesting, plunger rod assembly,
A
labeling, safety device assembly
- Special topic: Needle protection labels and safety devices
11:00 Morning refreshments Markus K. Hoersch
Technical Sales Manager
BAUSCH + STROEBEL
11:20 Toxicological risk assessment of leachable substances
from container-closure systems
• eneral background on leachables from container-closure systems
G 15:00 Regulatory issues relating to combination products
• egulatory expectations for the safety assessment of
R with delivery devices
leachable substances • Definition of “combination product”
• Current approaches to evaluate the potential for safety concerns • Regulatory paths for combination products / Primary Mode of Action
• orking examples to demonstrate how to conduct a
W • eCTD content planning for combination products with delivery devices
toxicological assessment • hallenges in eCTD content planning for combination products with
C
delivery devices
Stephen A. Barat, Ph.D.
Director, Toxicology and Operations Dr. Silke Conrad
Forest Research Institute Manager Regulatory Affairs
Ypsomed AG
12:00 Practical considerations for shipment of pre filled
15:20 Afternoon refreshments
syringes and experimental approaches taken
• Overview on practical consideration for shipment
• Shipping and handling charges
• Current practices in shipping and handling 16:00 Panel discussion: Evaluate benefits and challenges
of outsourcing
Amanda Wolf
Panelists will assess the importance of pharma-device alliances and design
Scientist
partnerships on pre-filled syringe products, discuss how to make most of the
Pfizer
partnership with contract manufacturers for any questions or participation
please contact sonia.tomar@visiongainglobal.com
12:40 Networking lunch
16:40 Chair’s closing remarks
16:50 End of Conference
6. Partners
2nd Prefilled Syringes Americas
April 5th - 7th 2011, USA
Associate Sponsor:
The BAUSCH + STROEBEL product range specializes Sponsorship and exhibition opportunities:
in machines for pharmaceutical primary packaging,
including equipment for washing, sterilizing / This event offers a unique opportunity to meet and do business
depyrogenating, filling, closing and labeling of containers such as ampoules,
cartridges, disposable syringes, vials and bottles of all kinds. Our systems are with some of the key players in the pharmaceutical and biotech
designed to comply with the latest FDA and GMP requirements and are available
for all capacity ranges, starting from laboratory testing and clinical batches to fully industries. If you have a service or product to promote, you can
integrated commercial production. With more than 40 years of experience and over
10,000 machines delivered BAUSCH + STROEBEL is a leading manufacturer of high- do so at this event by:
quality equipment for the pharmaceutical industry.
For further information please visit: www.bausch-stroebel.com • Hosting a networking drinks reception
Optima Group pharma is comprised of the trademarks Inova, Klee,
Kugler and effective January 1, 2011 Metall + Plastic. First-class • Taking an exhibition space at the conference
pharmaceutical filling, closing and freeze-drying now united
with isolator technology. Optima Group pharma manufactures • Advertising in the delegate documentation pack
cGMP compliant standard and custom filling, closing, processing,
freeze drying and isolator equipment for the pharmaceutical industry. Offering • Providing branded bags, pens, gifts, etc.
an immensely diversified and innovate range of solutions. We do believe: Optima
Group pharma is your ideal partner – also for the efficient and precise realization of If you would like more information on the range of
complex turnkey projects.
For further information please visit: www.optima-packaging-group.de sponsorship or exhibition possibilities for visiongain's
SCHOTT forma vitrum is one of the world’s leading suppliers
2nd Prefilled Syringes Americas Conference,
of parenteral packaging for the pharmaceutical industry.
More than 600 production lines in 14 countries worldwide
please contact us.
produce 7 billion syringes, vials, ampoules, cartridges and
special articles made of tubing glass or polymer. Excellent raw materials, state-of-
the art manufacturing, the use of the latest technologies, continuous research and Ronald Magali, +44 (0)20 7549 9934
development enable innovative product solutions that meet our customers‘ stringent
demands. The back-up possibilities offered by our production sites situated all over ronald.magali@visiongainglobal.com
the world provide flexibility, reliability and security to our partners.
For further information please visit: www.schott.com
Media Partners:
PharmiWeb.com is the leading industry-sponsored portal for
the pharmaceutical sector. Supported by most of the leading
pharmaceutical corporations, PharmiWeb.com provides dynamic real-time news, features,
events listings and international jobs to industry professionals across Europe and the US.
About visiongain:
For further information please email: corporate@pharmiweb.com Visiongain is a specialist business information company focused on
BIOTECHNOLOGY EUROPE is owned by BIOTECHNOLOGY providing cutting edge products and services across the Pharmaceutical/
WORLD. It is based and located in Warsaw, Poland.
Biotech, Telecommunications, Defence and Finance sectors, which
Biotechnology World was founded in 2007 to provide the world’s biotech and
pharma information and market to make it universally accessible and useful include reports, conferences, online daily news and offline news
for scientific and business processes. Its first step to fulfilling that mission was
building the BIOTECHNOLOGY EUROPE platform that will allow a quick spread of analysis and bespoke consultancy. With a commitment to innovation
information in different channels. BIOTECHNOLOGY EUROPE offers companies and excellence, visiongain offers flexible solutions to meet our clients’
completed internet public relations, publication and marketing solutions. One of the
mains goals of BIOTECHNOLOGY EUROPE is to integrate the Biotech and Pharma business intelligence needs, providing the right information at the
Sector in Europe to global biotechnology, pharmaceutical and life science activities.
right time to facilitate the commercial decision-making process. Our
For further information please visit www.biotechnology-europe.com
pharmaceutical products include Pharma Business Daily, the leading
InPharm is the online platform for exclusive pharmaceutical
news, comment, contracts, services, jobs and events and is daily email newsletter for the pharmaceutical, biotech and healthcare
home to InPharmjobs.com, Pharmafile and Pharmafocus.
For further information please visit: www.In-Pharm.com industries, and a range of independent, high-quality, in-depth reports
Future Pharmaceuticals has forged powerful relationships
Driving the Industry Forward | www.futurepharmaus.com covering focused and topical areas of concern. Our pharmaceutical
with key industry leaders to provide a platform for successful conferences address the hottest commercial, regulatory and technical
brand recognition, and for senior decision-makers to have the means to procure and
plan implementation strategies based on the topics covered. Positioned to be an topics and provide an ideal forum for debate and networking for
authoritative resource within top pharma companies as well as small, specialty, and
biotech, Future Pharmaceuticals magazine is geared to create a deep penetration
pharmaceutical professionals from around the world.
into a highly targeted and responsive audience, bridging the gap between the
For further information, please visit: www.visiongain.com
industries’ top issues and the solutions top-tier vendors can provide.
For further information please visit: www.futurepharmaus.com
7. Registration Form
2nd Prefilled Syringes Americas
April 5th - 7th 2011, USA
Conf. code VG
Standard Prices
Conference and workshop Fee: £1699 (USD* 2629)
2nd Prefilled
Conference only
Workshop only
Fee:
Fee:
£1299
£599
(USD* 2010)
(USD* 927)
Syringes Americas
Number of bookings: Total cost:
April 5th - 7th 2011
*USD price is estimate only
USA
Promotional Literature Distribution
Distribution of your company’s promotional literature to all conference attendees
Fee: £999 VAT: £199.80 Total: £1198.80
How to book
Details
Email: conferences@visiongainglobal.com
Forename: Surname: Web: http://www.visiongain.com/pfsamericas
UK Office:
Job Title: Company: Tel: +44(0) 20 7336 6100
Fax: +44(0) 20 7549 9932
Main Switchboard Number: Visiongain Ltd
BSG House
226-236 City Road
Address: London
EC1V 2QY
UK
General information
Country: Postcode: Venue: TBA, USA
Payment terms: Visiongain require the full amount to be paid before the conference. Visiongain
Phone: Fax: Ltd may refuse entry to delegates who have not paid their invoice in full. A credit card guarantee
may be requested if payment has not been received in full before the event. Visiongain Ltd reserves
Email: the right to charge interest on unpaid invoices.
Substitutions/name changes or cancellations: There is a 50% liability on all bookings once
Signature: made, whether by post, fax, email or web. There is a no refund policy for cancellations received on or
after one month before the start of the event. Should you decide to cancel after this date, the full invoice
I confirm that I have read and agree to the terms and conditions of booking must be paid. Conference notes will then be sent to you. Unfortunately, we are unable to transfer places
between conferences. However, if you cannot attend the conference, you may make a substitution/name
change at any time, as long as we are informed in writing by email, fax or post. Name changes and
Methods of payment substitutions must be from the same company or organisation and are not transferable between
countries. Please note that discounted delegates places at a visiongain event are non refundable.
Payment must be made in sterling
Invoice alterations: There will be an administration charge of £50 for any changes to an invoice,
By Mail: Complete and return your signed registration form together with your cheque payable excluding substitutions/name changes, requested by the customer. This will be charged to the
to Visiongain Ltd and send to: visiongain Ltd, BSG House, 226-236 City Road, London, EC1V 2QY, UK customer by credit card prior to the changes being made.
Indemnity: Visiongain Ltd reserves the right to make alterations to the conference/executive
By Fax: Complete and fax your signed registration form with your credit card details briefing content, timing, speakers or venue without notice. The event may be postponed or cancelled
to +44 (0) 20 7549 9932 due to unforeseen events beyond the control of visiongain Ltd. If such a situation arises, we will try
to reschedule the event. However, visiongain Ltd cannot be held responsible for any cost, damage or
By Phone: Call us on +44 (0) 20 7336 6100 with your credit card details expenses, which may be incurred by the customer as a consequence of the event being postponed or
cancelled. We therefore strongly advise all our conference clients to take out insurance to cover the
By Credit Card: Fill in your card details below and fax back to +44 (0) 20 7549 9932
cost of the registration, travel and expenses.
By Bank Transfer: Data Protection: Visiongain Ltd gathers and manages data in accordance with the Data
Protection Act 1988. Your personal information contained in this form may be used to update you on
Visiongain Ltd A/C: visiongain Ltd visiongain Ltd products and services via post, telephone, fax or email, unless you state otherwise. We
Barclays Bank Sort Code: 20-71-64 may also share your data with external companies offering complementary products or services. If you
Piccadilly Branch Account No: 6038 7118 wish for your details to be amended, suppressed or not passed on to any external third party, please
send your request to the Database Manager, visiongain Ltd, BSG House, 226-236 City Road, London,
48 Regent Street Swift Code: BARC GB22 EC1V 2QY. Alternatively, you can visit our website at www.visiongain.com and amend your details.
London W1B 5RA, UK IBAN: GB80 BARC 20716460387118 Please allow approximately 30 days for your removal or update request to be applied to our database.
Following your removal or update request, you may receive additional pieces of communication from
Please debit my credit card: visiongain Ltd during the transitional period, whilst the changes are coming into effect.
Access MasterCard Visa American Express Fee: The conference fee includes lunch, refreshments and conference papers provided on the day.
This fee does not include travel, hotel accommodation, transfers or insurance, (which we strongly
recommend you obtain).
Card number: VAT: VAT will be charged at the local rate on each conference. Delegates may be able to recover VAT
incurred by contacting Eurocash Corporation plc +44 (0) 1273 325000, eurocash@eurocashvat.com.
Eurocash specialise in recovering cross-border VAT.
How we will contact you: Visiongain Ltd’s preferred method of communication is by email and
Expiry Date: phone. Please ensure that you complete the registration form in full so that we can contact you.
Security number (last 3 digits on back of credit card): Unable to attend
Obviously nothing compares to being there but you need not miss out. Simply tick the box and send
Signature: with your payment. You will receive speaker talks in PDFs two weeks after the event.
Yes, please send me speaker talks Price£550 VAT:£110 Total:£660
Cardholder’s name:
Office use only
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www.visiongain.com/pfsamericas