Product Description
This volume sets out precise definitions for over 180 terms commonly used when reporting adverse drug reactions to regulatory authorities and drug manufacturers. Compiled at the request of the pharmaceutical industry, the book aims to respond to the need for a standard international terminology that is specific to both the characteristics of adverse drug reactions and the procedures of post-makerting surveillance.
Product Details
- Amazon Sales Rank: #3216278 in Books
- Published on: 2000-03-28
- Original language:
English
- Binding: Paperback
- 146 pages