Targeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics

This book describes the authors’ standard or ‘best’ practices used in writing regul- ed clinical documents for the drug and biologics industry. The fundamental premise of this book is that the end (documents submitted to a health authority) is dep- dent on the beginning (the planning and strategy th...

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Bibliographic Details
Corporate Author: SpringerLink (Online service)
Other Authors: Wood, Linda Fossati (Editor), Foote, MaryAnn (Editor)
Format: Electronic eBook
Language:English
Published: Basel : Birkhäuser Basel, 2009.
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Online Access:Full Text via HEAL-Link

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