Hi, everyone i am providing you the best presentation about the Pakistan relate Drug regulatory affairs and the concept of regulatory affairs of Pharmaceuticals
The Regulatory Affairs Associate will provide the internal regulatory affairs support for development and post-marketing of Class II and III medical devices.
Career Opportunities in the Clinical Research IndustryAccess-Pharma Jobs
Career Opportunites in Clinical Research, Regulatory Affairs, and Pharmacovigilance. International Clinical Research Academy and Access Clinical Research
Hi, everyone i am providing you the best presentation about the Pakistan relate Drug regulatory affairs and the concept of regulatory affairs of Pharmaceuticals
The Regulatory Affairs Associate will provide the internal regulatory affairs support for development and post-marketing of Class II and III medical devices.
Career Opportunities in the Clinical Research IndustryAccess-Pharma Jobs
Career Opportunites in Clinical Research, Regulatory Affairs, and Pharmacovigilance. International Clinical Research Academy and Access Clinical Research
DRA (Drug Regulatory Affairs) , RA (Regulatory Affairs)Naman Ruhela
A Brief Introduction about the Regulatory Affairs / Drug Regulatory Affairs (DRA). Introduction to Drug Regulatory Affairs. Why Drug Regulatory Affairs?. Role of Regulatory Affairs Experts. Types of the company hiring RA professionals. RA professional can get employment. Regulatory Bodies.
Drug Regulatory Affairs By Mr. Pankaj DhapadePankaj Dhapade
This presentation covers basic understandings of regulatory affairs profession. It contains,
1. Introduction of Regulatory Affairs
2. Why Drug Regulatory Affairs
3. Role of Regulatory Affairs Experts
4. Qualities of Regulatory Affairs Expert
5. Qualities for Submission Management
6. Regulatory Bodies
Clinical research : Drug regulatory affairs and Pharmacovigilance.ProfDnyaneshwariJosh
Schedule Y, FDA, Appendices, Post marketing surveillance,Clinical trial,WHO,ICH-GCP, FDA-CFR, Safety,Adverse Drug reaction, Adverse Event(AE), Serious Adverse Event(SAE),Reporting, IND , 3500A form
Fundamental concept of regulatory affairs in pharmaceutical & biotechnologyHitendra Singh
RA is a comparatively new profession which developed from the desire of governments to protect public health by controlling the Quality, safety and efficacy of products in areas including pharmaceuticals, Biotechnology, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
Goals of Regulatory Affairs Professionals:-
Protection of human health
Ensuring safety, efficacy and quality of drugs
Ensuring appropriateness and accuracy of product information
Raaj Global Pharma Regulatory Affairs Consultants Thane-mumbai profile-updat...Rajashri Survase Ojha
Raaj-GPRAC is a Thane-Mumbai (India) based agency.
Our offerings includes but not limited to making Regulatory filing strategy, Preparation of pharmaceutical product registration dossier, filing assistance, response to regulatory queries, life cycle management, regulatory compliance audit and Training.
We offer flexible and need based services to meet customer/client requirements so as to save time and cost.
Regulatory affairs in Pharmaceutical IndustryRama Shukla
Regulatory affairs is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and a member (as a higher/professional Education Institute) of Quality Council of India(QCI) -which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing. GMP in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.
Our group of learned professionals from above mentioned sectors of the pharma and healthcare industries have put together their knowledge; know about and practical experiences in form of this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training & distance and e-learning platform provider for pharmaceutical and healthcare professionals in the aeas of GMP, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. The importance of quality healthcare is known to our founders and thus numerous efforts are being made to offer friendly but effective and easy online/distance sources of GMP information, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of online seminars, distance/online courses as well as training programmes along with knowledge of worldwide affairs of the industry; in short a round-the-clock help for any information in these areas needed by anybody from around the world. Based on high standard of quality, the training programmes in Pharma and healthcare GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management etc areas have been approved and certified by Quality Council of India.
The IGMPIs team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and healthcare manufacturing easily accessible, through this platform.
Greetings from Virtue Insight,
I am happy to invite you and your colleagues to be a sponsor/ delegate for our upcoming “9th Pharmacovigilance 2015” The conference will Be held on 2nd September 2015, Kohinoor Continental Hotel, Mumbai, India. Please find the detailed agenda for the same with this email.
FMD:- + 91 9171350244 or deepak@virtueinsight.co.in, deepakrajvirtueinsight@gmail.com
DRA (Drug Regulatory Affairs) , RA (Regulatory Affairs)Naman Ruhela
A Brief Introduction about the Regulatory Affairs / Drug Regulatory Affairs (DRA). Introduction to Drug Regulatory Affairs. Why Drug Regulatory Affairs?. Role of Regulatory Affairs Experts. Types of the company hiring RA professionals. RA professional can get employment. Regulatory Bodies.
Drug Regulatory Affairs By Mr. Pankaj DhapadePankaj Dhapade
This presentation covers basic understandings of regulatory affairs profession. It contains,
1. Introduction of Regulatory Affairs
2. Why Drug Regulatory Affairs
3. Role of Regulatory Affairs Experts
4. Qualities of Regulatory Affairs Expert
5. Qualities for Submission Management
6. Regulatory Bodies
Clinical research : Drug regulatory affairs and Pharmacovigilance.ProfDnyaneshwariJosh
Schedule Y, FDA, Appendices, Post marketing surveillance,Clinical trial,WHO,ICH-GCP, FDA-CFR, Safety,Adverse Drug reaction, Adverse Event(AE), Serious Adverse Event(SAE),Reporting, IND , 3500A form
Fundamental concept of regulatory affairs in pharmaceutical & biotechnologyHitendra Singh
RA is a comparatively new profession which developed from the desire of governments to protect public health by controlling the Quality, safety and efficacy of products in areas including pharmaceuticals, Biotechnology, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
Goals of Regulatory Affairs Professionals:-
Protection of human health
Ensuring safety, efficacy and quality of drugs
Ensuring appropriateness and accuracy of product information
Raaj Global Pharma Regulatory Affairs Consultants Thane-mumbai profile-updat...Rajashri Survase Ojha
Raaj-GPRAC is a Thane-Mumbai (India) based agency.
Our offerings includes but not limited to making Regulatory filing strategy, Preparation of pharmaceutical product registration dossier, filing assistance, response to regulatory queries, life cycle management, regulatory compliance audit and Training.
We offer flexible and need based services to meet customer/client requirements so as to save time and cost.
Regulatory affairs in Pharmaceutical IndustryRama Shukla
Regulatory affairs is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, veterinary medicines, medical devices, pesticides, agrochemicals, cosmetics and complementary medicines.
Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and a member (as a higher/professional Education Institute) of Quality Council of India(QCI) -which is an autonomous body and an accreditation authority for education & vocational training providers under the Department of Industrial Policy & Promotion, Ministry of Commerce & Industry, Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches. GMP- is an essential element of industries like pharmaceutical, cosmetic, Ayurveda, biotech, homeopathic, medical device and food manufacturing. GMP in itself is the most dynamic part which witnesses frequent changes in terms of newer rules being added and older ones being renewed. Keeping self updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices.
Our group of learned professionals from above mentioned sectors of the pharma and healthcare industries have put together their knowledge; know about and practical experiences in form of this GMP guide. IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training & distance and e-learning platform provider for pharmaceutical and healthcare professionals in the aeas of GMP, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice and Product Management. The importance of quality healthcare is known to our founders and thus numerous efforts are being made to offer friendly but effective and easy online/distance sources of GMP information, Quality Assurance and Control, Pharma and healthcare Regulatory Affairs, Clinical Research, Pharmaceutical IPR and Good Laboratory Practice in form of online seminars, distance/online courses as well as training programmes along with knowledge of worldwide affairs of the industry; in short a round-the-clock help for any information in these areas needed by anybody from around the world. Based on high standard of quality, the training programmes in Pharma and healthcare GMP, Quality Assurance and Quality Control, Regulatory Affairs, IPR, Pharma Product Management etc areas have been approved and certified by Quality Council of India.
The IGMPIs team of technology experts and other Industry advisors together pursue to make cGMP knowledge, training in the area of Pharma and healthcare manufacturing easily accessible, through this platform.
Greetings from Virtue Insight,
I am happy to invite you and your colleagues to be a sponsor/ delegate for our upcoming “9th Pharmacovigilance 2015” The conference will Be held on 2nd September 2015, Kohinoor Continental Hotel, Mumbai, India. Please find the detailed agenda for the same with this email.
FMD:- + 91 9171350244 or deepak@virtueinsight.co.in, deepakrajvirtueinsight@gmail.com
Do you know how many rewarding job opportunities exist in the Clinical resea...Access-Pharma Jobs
If you are a BSc/MSc/PhD or MD/PharmD in career change, you can see some of the available career opportunities in the Clinical research industry and how to get in this field in this presentation made on Jan 14, 2017 at the Pharmacolloque 2017:
https://cra-school.com/news/
Greeting From Virtue Insight,
I am happy to invite you and your colleagues to be a sponsor/ delegate for our upcoming “9th Pharmacovigilance 2015” The conference will be held on 2nd September 2015, Kohinoor Continental Hotel, Mumbai, India.
KEY SPEAKERS:-
• V. Kalaiselvan, Principal Scientific Officer, Indian Pharmacopoeia Commission Ministry of Health and Family Welfare Govt. of India
• Arun Bhatt, President, ClinInvent Research
• Deepa Arora, Vice President - Pharmacovigilance & Global Head - Drug Safety & Risk Management, Lupin
• Bhaswat Chakraborty, Senior Vice President, Cadila
• Babita Kirodian, Head of Country Pharmacovigilance, Bristol Myers Squibb
• Nipom Deka, Regional Pharmacovigilance Manager, Asia, Africa & Middle East, Abbott
• Shashidhar Swamy, Head Pharmacovigilance, Wockhardt
• Mohammad Salim, Country Safety Lead, Pfizer
• Manish Verma, Director Medical Affairs, Sanofi
• Karthik Babu, Affiliate Pharmacovigilance Head, Sanofi
• Chirag Trivedi, Director & Head of Clinical Study Unit, Sanofi
• Priya Chatterjee, Director - Regulatory Affairs, Merck Serono
• Milind Antani, Partner In-Charge - Pharma LifeSciences, Nishith Desai Associate
• Anand Harugeri, Patient Safety and Regulatory Affairs Manager, Astrazeneca
• Deepti Sanghavi, Assistant Manager - Medical Writing, Tata Consultancy Services
• Sandeep Sewlikar, Manager – Clinical Affairs, Johnson and Johnson
• Girish Parhate, Head Regulatory Affairs, Bayer Pharmaceuticals
• Rajashri Survase Ojha, Founder and MD, Raaj GPRAC
• Vandana Jolad, Director, VIaTal Pharma
Plus Many More...
CONFERENCE BOOKING DETAILS:-
• Early Bird Discounted Price - Conference Delegate Pass (INR 6,000 + Tax (14%) per delegate) - Book and Pay before 20th July 2015 avail the early bird discounted price. You can simply email or call and book your conference delegate seats on TEL: +91 9940043915. Email – swetha@virtueinsight.co.in
• Standard Price after Early Bird Discounted Time – 1 or 2 Delegates (INR 7,000 + Tax (14%) per delegate) - You can simply email or call and book your conference delegate seats on TEL: +91 9940043915. Email – swetha@virtueinsight.co.in
• Group Discounts – 3 or 4 Delegates - (INR 6,500 + Tax (14%) per delegate)
• Group Discounts – 5 or more Delegates - (INR 5,000 + Tax (14%) per delegate)
• Conference Sponsor & Exhibition Stall - Should you wish to Sponsor, or purchase a Exhibition Stall (Booth) or a paid Speaker Slot, you can simply email your interest and queries to TEL: +91 44 65515695, +91 9940043915 or swetha@virtueinsight.co.in
In case you or any of your colleagues might be interested in participating in the same, please let me know and I will be happy to call you and help you with the registration.
Thank you for your time and consideration. I look forward to hearing from you
Thanks,
Swetha
Strategies for Conducting New Product Scientific Assessment - Yavuz SILAY - D...Yavuz Silay
Strategies for Conducting New Product Scientific Assessment - Due Diligence - New Strategies for Successful Licensing Acquisitions , DIA , Session Panel, June 22 2008,
Biotechnology consulting refers to the practice of organization involved in Pacificlinkconsulting services contact: San Diego, CA 92127 Phone: 858-335-1300
Regulatory, Quality & Clinical Due Diligence: The Oft Overlooked Keys to Suc...Michael Swit
June 23, 2010 webinar sponsored by The Weinberg Group, with an emphasis on key issues to explore during due diligence in acquiring FDA-regulated products or companies.
Practice Areas: New Product Planning, Business Development and Licensing, Commercial Strategy and Analytics, and Epidemiology and Forecasting.
Our boutique expertise is focused on elucidating patient benefits of bio-pharmaceutical products, medical devices, and businesses. With insightful strategies and solutions aimed at planning and growing our clients’ business, our mission is to continue being the “go-to” firm and preferred partner for our clients in their commercial planning and R&D initiatives.
Our chief operating principle is an unsurpassable commitment to quality and our philosophy has been to develop and sustain strong long-term relationships with clients based on an in-depth understanding of client needs, rigorous research, sound methodologies, and keeping ahead of industry developments.
It includes information about regulatory bodies, role of drug Regulatory professional, countries with their regulatory bodies, intellectual property rights, terminologies related to DRA, drug approval process, event regarding lack of Drug regulatory affairs
The 10 Most Innovative Pharma and Biotech Solution Providers, 2020 September ...Merry D'souza
The 10 most innovative pharma and biotech solution providers, 2020 september 2020; Insights Success has published The 10 most innovative pharma and biotech solution providers.
The 10 Most Innovative Pharma and Biotech Solution Providers, 2020 September ...
Regulatory Affairs 2010
1. Speid & Associates, Inc.
Consultancy Services, Inc.
Lorna Speid, Ph.D., RAC
President
Speeding New Drugs to Market®
www.drugstomarket.com
2. Speid & Associates, Inc.
Speid & Associates is a regulatory affairs
and drug development consultancy
- Dr. Speid is the principal consultant
- Associates with extensive experience in
regulatory affairs and drug development
are placed on projects as needed
- The associates are based in different
countries as well as in the United States –
most have some large pharma
experience
3. Speid & Associates, Inc.
The company is a US-based California
corporation
The clientele is US-based and international
The company has collaborations and
partnerships with other reputable
companies to provide high quality services
in relevant areas of drug development to
Speid & Associates clients
4. Dr. Speid’s Credentials
Registered UK Pharmacist
B.Pharm.(Hons.) – King’s College, London University
Ph.D. from University of Wales & Centre for Medicines
Research International (UK)
Experience working for a number of international
pharmaceutical companies, including:
- Sanofi-Winthrop (UK)
- Ciba-Geigy/Novartis (HQ - Switzerland)
- GeneMedicine/Valentis, Inc. (US) - Dir. Reg Affairs
- NewBiotics (Officer of the Company), VP Regulatory Affairs &
Project Management [incl. clinical & QA])
- Avera (Officer of the Company), VP Regulatory Affairs
5. Dr. Speid’s Expertise
Dr. Speid has very broad-based experience
- with international pharmaceutical industry
- as core team member of international project teams in large and small pharmaceutical
organizations
- setting up and managing project teams, including virtual teams
- with FDA and health authorities worldwide (CDER & CBER)
- with all major health authorities worldwide
- With INDs, MAAs, NDAs, CTDs
- Document management oversight experience
- Appeals procedures
- Has set up and monitored clinical trials in past, and therefore understands the clinical
process
- Good understanding of challenges faced by small and large companies – ability to
address these to optimize the potential for success in the small company setting
- A summary of case studies is available towards the end of this
presentation
6. Dr. Speid’s Bio
Lorna Speid, B.Pharm. M.R.Pharm.S., Ph.D., RAC is President of Speid &
Associates, Inc. a regulatory and drug development consultancy based in San
Diego, California. She works with small and large pharmaceutical companies,
assisting them at the various stages of the drug development process, including
European strategic regulatory affairs.
Dr. Speid began her career as a pharmacist in the UK, after which she completed
a Ph.D. at the Center for Medicines Research International, into the Safety
Assessment of Medicines, Pre and Post Marketing. She has worked for large as
well as small pharma companies, including Sanofi Winthrop in the UK (now Sanofi-
Aventis), Ciba Geigy and Novartis in Switzerland. Small companies that she has
worked for include Valentis, Inc., NewBiotics, and Avera, Inc., the last two
companies at Vice President of Regulatory Affairs level.
She has a Bachelor of Pharmacy degree from the University of London, and a
Ph.D. from the University of Wales, College Cardiff.Document management
oversight experience.
Dr. Speid is the author of Clinical Trials: What Patients and Healthy Volunteers
Need to Know – published by Oxford University Press.
7. Associates
US and international located
Wide range of skillsets [drugs, biologics,
diagnostics, devices, statistics, clinical,
marketing, EU/US/international]
Experienced regulatory and drug development
professionals
- Most have large pharma experience
- Most have achieved Vice President level or Sr.
Director level
Associates are assigned to projects as needed
8. Why Hire Us?
We believe that a
successful development
program requires more than
serendipity or luck
--- We have a proven track
record of past
achievements
9. Why Hire Us?
We work with our clients to
achieve successful global
registration, as
expeditiously as possible
--- help the client to put the
pieces of the development
jigsaw together
successfully.
10. Why Hire Us?
We can help you to
determine what your next
move should be with a NCE
or established drug,
biological, device or
diagnostic
11. Why Hire Us?
We can ‘jump start’ a stalled
program:
-Clinical holds
- Rejected marketing
applications (for any health
authority in the world)
-Dr. Speid has appeals
experience and a
proven track record of
success in this area
12. How We Work
Strategic
Tactical
Hands-on
We can work on location or remotely
- Our clients are as far away as in Australia, or as
local as San Diego
Dr. Speid is available to act as a consultant
Vice President of Regulatory Affairs on an as
needed basis
13. Types of Customers
Customer base
- Small companies
- Large pharma
- US based companies
- Companies in Canada, Europe, Australia and rest of
world
- Venture capital organizations
- Analysts
- Angel investor organizations
- Financial institutions, including Wall Street
14. Overview of Services
Clinical trial applications – for individual
European countries, and other countries
Investigational New Drug Applications
Orphan Drug Applications
New Drug Applications (electronic and paper
Common Technical Dossier formats)
Marketing Authorization Applications
(electronic and paper Common Technical
Dossier formats)
15. Overview of Services cont.
Abbreviated New Drug Application (ANDA)
Premarket Approvals (PMA)
510k applications
505(b)(2) applications
Fast Track applications
Development of meeting strategy and briefing
package preparation
- End of Phase 1 / End of Phase 2 meetings
- Pre-NDA meeting
16. Overview of Services cont.
Special Protocol Assessment strategy development
Special Protocol Assessment preparation
Pediatric strategy development
- US
- Europe
- International
Marketed product support
Postmarketed product support
US Agent services for ex-US companies
17. Overview of Services cont.
Regulatory authority meeting strategy
development
- Pre-IND
- Pre-IDE
- End of Phase 2 meeting
- Informal discussions with reviewers
- Pre-NDA meeting
- Meetings during NDA / Marketing Authorization
Application review
18. Overview of Services –
Types of Projects
Drugs (small molecule)
Biologics (large molecule)
Gene Therapy
Medical Devices
In vitro Diagnostics
Combination Products
Generics
Due Diligence
Quality Assurance including audits [through partners]
Strategic medical writing
19. Overview of Services –
Therapeutic Areas
Experience with many therapeutic areas,
including:
- Anti-infective
- Oncology – gastric, colorectal, pancreatic, head and
neck, hematological
- Respiratory
- Women’s health
- Dermatology
- Anti-inflammatory and immunological diseases
- Central nervous system
- Bone
20. Overview of Services – Due
Diligence
Conducted for companies, VCs and financial
institutions
- Review of company strategy
- Review of the compounds
Extensive review of documents, including regulatory
correspondence
Review of regulatory actions, e.g. warning letters
- Assessment of the company systems and management team
- Assessment of risk and probability of success
- Assessment of the regulatory hurdles, and time to market
- Preparation of report
21. Overview of Services -
Clinical
Review of Summary Bases of Approvals
Preparation of INDs, CTAs, IDEs
Set up clinical trials
Writing of Investigator’s Brochures
Writing, editing or review of Protocols
Submissions to IRBs and FDA
Preparation of Informed Consent Documents
Writing, editing and/or review of clinical study
reports
22. Overview of Services –
Devices and Diagnostics
Strategic and hands-on
US and European
- Relationship building with FDA
- Relationship building with Notified Bodies
Rest of the world
Health authority meeting requests and
preparations
- Briefing package preparations
Clinical protocol design and preparation
IRB/ethics committee liaison
23. Overview of Services -
INDs
Assistance and advice in clinical hold situations
Regulatory due diligence for licensing-in or
licensing-out situations
Preparation of IND Annual Reports
Advice regarding Quality Assurance issues
Preparation of IND safety reports
Preparation of INDs in the new eCTD format
Preparation of INDs in the older 9 section
format
24. Overview of Services –
Clinical Trial Applications
Expertise in new European Clinical Trial
process [European Clinical Trial Directive]
- Conversion of US IND to European Clinical Trial
Application
- Clinical trials for Russia and other Eastern
European countries via partners
- Clinical trial applications for China via partners
25. Overview of Services –
Toxicology
Review of toxicology guidelines
Development of toxicology strategy
- Acute toxicology study designs
- Sub-chronic toxicology study designs
- Chronic toxicology study designs
- Reproductive toxicology study designs
- Carcinogenicity study designs and strategy
Liaison with major toxicology houses
Preparation of toxicology protocols
Review of toxicology reports
Development of Pre-IND meeting strategy and
discussions with health authorities around the
toxicology issues
26. Overview of Services –
electronic CTDs
Building of global eCTD strategy
Organization of the internal and external
project teams
Interpretation of the guidelines for the
compound in question
Organization of discussions with Health
Authorities
Publishing strategy derivation
Expert writing
27. Global and International
Regulatory Affairs
See separate presentation about this service
offering:
- Europe
Japan
- USA
- South Africa
- Australia
- Eastern Europe
- South America
- Africa and Middle East
- Asia including China and India
28. Partnerships
Speid & Associates, Inc. has partnered with several
organizations in various parts of the world to bring
services to our clients. Please ask if you would like
additional information about the following:
- Life science services based in China – all aspects are available
- Document management services
- Clinical Research Organizations
- GLP toxicology services
- Analytical services
- Bankers, auction specialists, and fund raising specialists – preclinical -
Phase 2 data
- Specialized predictive individualized therapy services – for oncology and non
oncology drugs
- Notified Bodies
29. Case Studies
Dr. Speid worked with a small virtual organization to develop the
regulatory strategy for a combination product . This involved being the
main point of contact for the Division Head at FDA. Dr. Speid was
instrumental in ensuring that the virtual team understood the
requirements for the product development concept. She wrote the Pre-
Investigational Drug Exemption meeting request and the Pre-
Investigational Drug Exemption briefing document.
------------------------------------------------------------------------------------------------------
Dr. Speid worked with a late stage company that was licensing in a drug
with a large amount of disorganized documentation. She created an
internal document that identified the document management needs of the
organization. Several vendors were brought into the company to present
their services. The best document management vendor was selected
after internal support was garnered for the document management
system.
30. Case Studies
Dr. Speid created an NDA plan for a pharmaceutical company which had
licensed in a late stage haematological drug. Detailed operating plans
were put into place which included expert author meetings to assure the
creation of effectively written sections of the New Drug Application in
eCTD format.
------------------------------------------------------------------------------------------------------
Dr. Speid worked on a regulatory and development strategy for an ocular
implant combination product. This involved liaising with the combination
division and the drug division within the FDA to seek advice on the
appropriate registration pathway in the absence of guidelines. Clear
guidance was provided to the client to clarify the development and
registration pathway.
31. Case Studies
Negotiated with health authorities as part of key regulatory meetings to
avoid the need to repeat or to conduct new toxicological studies. This
saved the company at least 6 months and approximately 500, 000 USD.
--------------------------------------------------------------------------------------------------
Acted as the US Agent for a German company. Filed safety reports to the
FDA for two studies that were ongoing in Germany.
-----------------------------------------------------------------------------------------------------
Developed a regulatory strategy for a pediatric development which
involved US and European pediatric development for a monoclonal
antibody. This included consideration of the use of a parallel advice
procedure between the US and Europe.
--------------------------------------------------------------------------------------------
32. Case Studies
Wrote a strategic briefing document for a large and mid-size
pharmaceutical company for a drug intended for an autoimmune disease.
This document was used as the basis for a meeting with the FDA. The
meeting was successful and opened the way for a potential approval.