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2009-12-09T00:00:00.000Z

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Wrong John Berridge?

Dr. John C. Berridge

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Background Information

Employment History

Senior Regulatory Consultant

Pfizer Inc

Vice President

Santarus , Inc.

Affiliations

Technical Advisor
The International Society for Pharmaceutical Engineering Inc

Technical Advisor
Facility of the Year

Asia-Pacific Regulatory Affairs Advisor
Sanitron Industries Pte Ltd

Advisor
Steering Committee

Education

PhD

Web References (66 Total References)


Djicyice.com - Promoting quality in drug manufacturing: FDA is re-engineering the CMC review process for innovator and generic drugs and backing risk-based ICH quality standards

www.djicyice.com [cached]

If a manufacturer can demonstrate a good understanding of key product attributes (e.g., stability, bioavailability) and provide evidence that it can control critical variables and detect product deviations, regulatory authorities will be able to review applications in one review cycle, permit improvements in a manufacturing process without prior approval, and implement a risk-based inspection process, explains Pfizer Vice-President John Berridge.


ISPE Appoints John Berridge, PhD, as European Regulatory Affairs Advisor | ISPE Blog - News and information from the International Society for Pharmaceutical Engineering

blog.ispe.org [cached]

ISPE Appoints John Berridge, PhD, as European Regulatory Affairs Advisor ISPE Appoints John Berridge, PhD, as European Regulatory Affairs Advisor | ISPE Blog - News and information from the International Society for Pharmaceutical Engineering

...
ISPE Appoints John Berridge, PhD, as European Regulatory Affairs Advisor
ISPE has appointed John Berridge, PhD, as Europe Regulatory Affairs Advisor. He will take the post 1 February 2008. In this position Berridge will assist ISPE in its interactions with European regulatory authorities as well as helping to move forward ISPE's new Product Quality Lifecycle Implementation (PQLI) initiative.ISPE, which has Members from 90 countries, provides a neutral forum for industry, regulatory agencies, academics and individuals to exchange practical experience, collaborate and communicate.
"Along with Joe Phillips, our International Regulatory Affairs Advisor, and
Bob Tribe, Asia Pacific Regulatory Affairs Advisor, John now completes a team that is second to none," saidBob Best, President and CEO of ISPE.
...
Berridge retired from Pfizer Global Research and Development at Sandwich, England at the end of January 2006 as European Vice President of Pharmaceutical Sciences. Since then he has been a consultant and advisor to a portfolio of international clients, and a leader and visionary in ISPE's Product Quality Lifecycle Implementation (PQLI) initiative, which was launched in 2007.
...
Berridge was involved in the ICH processes from their inception, representing EFPIA in the quality topics discussions. He has contributed to guidelines on impurities in drug substances and their dosage forms, specifications, was the industry rapporteur for the Common Technical Document (Quality) and was the rapporteur for the Pharmaceutical Development Guideline (Q8 and its addendum which reached Step 2 in November of this year). At FIP's 55th World Congress in Stockholm in 1995 he was presented with an IPS award for his outstanding contribution to industrial pharmacy, and in September 1997 he was awarded the Royal Pharmaceutical Society Chiroscience award for his services to the pharmaceutical industry and for his work within ICH.


Douglas Ellsworth named ISPE’s Regulatory Affairs Advisor | ISPE Blog - News and information from the International Society for Pharmaceutical Engineering

blog.ispe.org [cached]

Ellsworth joins ISPE's two other Regulatory Affairs Advisors, John Berridge and Bob Tribe.

...
John Berridge, PhD, is ISPE's European Regulatory Affairs Advisor, assisting ISPE in its interactions with European regulatory authorities as well as helping to move forward ISPE's new Product Quality Lifecycle Implementation (PQLI) initiative. Berridge retired from Pfizer Global Research and Development at Sandwich, England at the end of January 2006 as European Vice President of Pharmaceutical Sciences.


Speakers' Biographies - INTERPHEX Asia 2009 ISPE Singapore Conference 2009

v1.interphexasia.showsite.rxnova.com [cached]

Dr. John Berridge European Regulatory Affairs Advisor ISPE

John retired from Pfizer Global Research & Development at Sandwich in January 2006 as Vice President of Pharmaceutical Sciences. He spent more than 31 years at Pfizer, starting as an Analytical Chemist, and ultimately responsible for all aspects of the product realisation disciplines of chemistry, pharmacy, analytical and regulatory CMC in Europe.
His research interests have been directed towards high performance liquid chromatography, with special emphasis on the use of chemometrics. This research was recognised by the award of the Chromatographic Society's Jubilee medal in 1989.
John was involved in the ICH processes from their inception until November 2007, representing EFPIA in the Quality topics discussions. He has contributed to guidelines on impurities in drug substances and their dosage forms, specifications, and the Common Technical Document (Quality): he was the Industry rapporteur for the pharmaceutical development guideline (Q8). In 1995 he was presented with an FIP IPS award for his outstanding contribution to industrial pharmacy and in 1997 he was awarded the Royal Pharmaceutical Society Chiroscience award for his services to the pharmaceutical industry. John now acts as an independent consultant and as European Regulatory Affairs Advisor to ISPE.
John will be presenting in Manufacturing Excellence: "Product Quality Lifecycle Implementation (PQLI) initiative - An Update" on 2 June 2009, Tuesday.


Conference Speakers Biographies | ISPE

www.ispe.org [cached]

John Berridge

...
John Berridge, PhD, retired from Pfizer Global Research and Development at Sandwich at the end of January 2006 as vice president of pharmaceutical sciences.He spent more than 31 years at Pfizer, starting as an analytical chemist, and more recently responsible for all aspects of chemistry, pharmacy, analytical, and regulatory CMC in Europe.His research interests have been directed toward high-performance liquid chromatography, with special emphasis on the use of chemometrics to aid method development.More than 40 papers and a book have been published and this research has been recognized by the award of the Chromatographic Society's Jubilee medal in 1989.Berridge has been involved in the ICH processes from their inception, representing EFPIA in the quality topics discussions.He has contributed to guidelines on impurities in drug substances and their dosage forms, specifications, was the industry rapporteur for the Common Technical Document (Quality) and is currently the industry rapporteur for the pharmaceutical development guideline (Q8).At FIP's 55th World Congress in Stockholm in 1995 he was presented with an IPS award for his outstanding contribution to industrial pharmacy, and in September 1997 he was awarded the Royal Pharmaceutical Society Chiroscience award for his services to the pharmaceutical industry and for his work within ICH.Berridge now works as a consultant, representing Pfizer at EFPIA, and thus will continue to support the ICH activities.

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