Good clinical practice guidelines providing an international quality standard for the regulation of clinical trials. This title is one of the "RPS Pharmacy Business Administration Series" which aims at covering all business aspects relating to pharmacy practice. Good Clinical Practice is an international quality standard for the regulation of clinical trials. GCP guidelines include standards on how clinical trials should be conducted, provide assurance of safety and efficacy of newly developed drugs and protect human rights. This text aims to be a one-stop source for guidance and checking the rules for proper conduct of clinical trials. It also includes historical development, trends, review of current system and future development.
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Selected for "The First Clinical Research Bookshelf" - Essential reading for clinical research professionals. a readable introductory summary of Good Clinical Practice (GCP) for pharmaceutical studies based on U.S. regulations and ICH E6 guidelines, which FDA has adopted as guidance...the book strikes a good balance between too much and too little detail --Norman M. Goldfarb, Journal of Clinical Research Best Practices Vol. 7(7), July 2011
...details requirements and discusses ethics surrounding clinical investigational trials. This is a worthy topic and relevant to pharmacy practice...an appropriate book for someone new to research, interested in doing research, or in an academic environment. --Barbara Lane Giacomelli, PharmD, MBA, BS, FASHP (Shore Memorial Hospital) Doody's Notes, November 2010
Good clinical practice guidelines providing an international quality standard for the regulation of clinical trials. This title is one of the "RPS Pharmacy Business Administration Series" which aims at covering all business aspects relating to pharmacy practice. Good Clinical Practice is an international quality standard for the regulation of clinical trials. GCP guidelines include standards on how clinical trials should be conducted, provide assurance of safety and efficacy of newly developed drugs and protect human rights. This text aims to be a one-stop source for guidance and checking the rules for proper conduct of clinical trials. It also includes historical development, trends, review of current system and future development.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : WorldofBooks, Goring-By-Sea, WS, Royaume-Uni
Paperback. Etat : Fine. N° de réf. du vendeur GOR014580871
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Vendeur : Better World Books, Mishawaka, IN, Etats-Unis
Etat : Good. Former library copy. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Includes library markings. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good. N° de réf. du vendeur 39023204-20
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Vendeur : Anybook.com, Lincoln, Royaume-Uni
Etat : Fair. This is an ex-library book and may have the usual library/used-book markings inside.This book has soft covers. In fair condition, suitable as a study copy. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,500grams, ISBN:9780853697909. N° de réf. du vendeur 9796092
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