Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices
autorzy: Gary Walsh, John J Tobin
nr: JWS00238
ISBN: 3527318771
ISBN13: 9783527318773
język publikacji: angielski
wydawca: Wiley
rok wydania: 2008
Hardcover
297 pages
Możliwość wysłania w ciągu 21 dni roboczych
Opis książki
Written in a clear and concise style by an experienced author, this attractively-priced book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices, making it the most comprehensive in its field.
Following a look at drug development, complete sections are devoted to national and EU regulatory issues, manufacturing license application and retention, and regulation in the USA. Other topics dealt with include CDER, CBER and marketing and manufacturing licenses, the ICH process and Good Laboratory/Clinical/Manufacturing Practices.
Everything pharmacologists, bioengineers, pharma engineers, students in pharmacy and those working in the pharmaceutical industry need to know about medical regulatory affairs.
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