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This profile was last updated on 9/1/2016 and contains contributions from the  Zoominfo Community.

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Herman Pieterse

Partner Fastinov Project

FASTinov

Email: h***@***.com

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I agree to the Terms of Service and Privacy Policy. I understand that I will receive a subscription to ZoomInfo Community Edition at no charge in exchange for downloading and installing the ZoomInfo Contact Contributor utility which, among other features, involves sharing my business contacts as well as headers and signature blocks from emails that I receive.

Background Information

Employment History

Coordinator Heerhugowaard

American Red Cross


Project Manager Biobone

Profess Medical Consultancy B.V.


Medical Director

Rhône-Poulenc S.A.


Position, Research and Development

Boehringer Ingelheim Corporation


Affiliations

NVFG

Pharmaceutical Scientist


DIA

Member


DARQA

Lid


Consultancy and Interim Management Agency PROFESSÂ Medical Consultancy B.V.

Founder


Governmental

Member


Education

Pharmacology

Free University


Web References(9 Total References)


CRAcademy

www.cracademy.com [cached]

Herman Pieterse
Herman Pieterse testimonial Herman Pieterse


CRAcademy: Meet the trainers

www.cracademy.com [cached]

Herman Pieterse


CRAcademy: Herman Pieterse testimonial

www.cracademy.com [cached]

Herman Pieterse testimonial
CRAcademy: Herman Pieterse testimonial Herman Pieterse testimonial Herman Pieterse


CRAcademy: Herman Pieterse

www.cracademy.com [cached]

Sue Fitzpatrick | Herman Pieterse
Herman Pieterse Herman Pieterse Herman Pieterse studied Pharmacology at the Free University in Amsterdam. In 1977 he joined Boehringer Ingelheim and held functions in Research and Development, like Clinical Research Manager for clinical pharmacology and International Medical Project leader for a cardiovascular research compound; He became Associate head of the Medical department. In 1984 he started working for Rhône-Poulenc as Medical Director and in 1988 he changed to Ovabloc Europe and took responsibility for international registration and research as Director of Regulatory Affairs and Technical/Clinical Research. In 1991 he founded the Consultancy and Interim Management Agency PROFESS® Medical Consultancy B.V. and assists now several major companies in the Health Care Industry with both regulatory and Quality Assurance issues, GCP clinical development and training. He was chief editor of a new book on "International Medical Devices Investigations" published by Interpharm Press Inc. in December 1997. In November 1996 Herman became a certified ISO 9000 Auditor. Herman is a member of the NVFG, DIA and DARQA. Herman was a member of the Governmental Working Party for the implementation of the European Clinical Trial Directive and academic consultant to the Pharmacology Department of the University of Ghent, Academic Medical Center in Amsterdam and the University Medical Center in Maastricht


CRAcademy: Testimonials

www.cracademy.com [cached]

Herman Pietersen


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