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- Sales Rank: #2071756 in Books
- Published on: 2011-07-22
- Original language: English
- Number of items: 1
- Dimensions: 9.00" h x .25" w x 6.00" l, .39 pounds
- Binding: Paperback
- 110 pages
About the Author
Patrick D. Stone, M.S. is an Ex-FDA, International Inspection Cadre for bioresearch monitoring (BIMO) and Drugs / TradeStone QA. He has 12 years experience as a Bioresearch monitor for the FDA. He conducts Domestic and International inspections of Clinical Investigators for pre-approval of pharmaceutical Drugs, Pharmaceutical Drug manufacturing plants and also conducts domestic Institutional Review Board investigations.
Most helpful customer reviews
0 of 1 people found the following review helpful.
Excellent writeup on the FDA
By Beboo
I recently have had the pleasure to interview Patrick Stone on my Clinical Trials Guru webshow, and we discussed this book, which eventually led me to actually read the book. As someone who has been in the clinical trials industry for about 10 years, I was always fascinated by the FDA and its inner workings. This book is really easy to read, and non-industry folks who are also interested in the FDA in general, will probably find its story flow non intimidating. A must read for anyone who ever wanted to know more about how the FDA works from both the Food as well as the Drug component.
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