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Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices PDF

298 Pages·2008·7.323 MB·English
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Description:
Written in a clear and concise by experienced authors, this book covers regulatory affairs in all major global markets for pharmaceuticals and medical devices.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.The book covers 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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Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.