Guide covering regulatory writing, audience analysis, and ethical responsibilities of biomedical writers. For students and practitioners. Softcover. DNLM: Writing.
Customer Reviews:
Avg. Customer Rating: 3.0 / 5.0
Useful for a newcomer to the clinical trial environment:
As a clinical trials computer programmer, I'm not the primary target audience for this book. However, as an experienced programming consultant who was new to clinical studies in the pharmaceutical industry, I found it gave me a useful overview of the typical deliverables that my efforts supported. Acronyms that are frequently used in the clinical environment, such as IB (Investigator's Brochure) and ISS (Integrated Safety Study) are given some definition and examples are shown. I found this information... more info
Not a practical guide, more a manifesto !:
Dr. Bonk is a seasoned professional who has worked at all levels of his craft, including the highest. This book is entitled "a practical guide for pharmaceutical research", and specifically concentrates on the output of documents from the pharmaceutical industry (regulatory documents and manuscripts, as well as, to a lesser extent, audio-visual preparations and computer-generated products). I bought the book because it was the only one that specifically addresses the needs of those of us working in the... more info
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