A01=Helene I. Dumitriu
affairs
Author_Helene I. Dumitriu
authorization
Category=VFD
clinical
clinical trial documentation
compliance auditing
development
dossier
eq_bestseller
eq_health-lifestyle
eq_isMigrated=1
eq_isMigrated=2
eq_nobargain
eq_non-fiction
global
marketing
medicinal
medicines regulation
pharmaceutical policy development
product
regulatory agency procedures
regulatory science
regulatory system quality assurance
trial
Product details
- ISBN 9781574910513
- Weight: 970g
- Dimensions: 178 x 254mm
- Publication Date: 30 Sep 1997
- Publisher: Taylor & Francis Inc
- Publication City/Country: US
- Product Form: Hardback
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Good Drug Regulatory Practices offers a series of policies and procedures to assure quality and timely regulatory submissions to national regulatory agencies. This book begins with introductory chapters describing the need for policy documentation, and the philosophy underlying the policies, and presents policies and standards that can be used as presented or adapted to individual situations in your company.
Dumitriu, Helene I.
