Author: Suzanne Parisian
Publisher:
ISBN:
Category : Law
Languages : en
Pages : 680
Book Description
Parisian (formerly of the Food and Drug Administration, now a consultant) offers a guide to preparing clinical trials intended for submission to the FDA and for marketing purposes. She also provides an organizational map of the agency, outlining its requirements, procedures, and history, with an emphasis on the implications for medical practice, manufacturing, and marketing. The logic governing the agency and the rationale by which it makes its decisions are included in the coverage. Annotation copyrighted by Book News Inc., Portland, OR.