募捐 9月15日2024 – 10月1日2024 关于筹款

Medical Product Regulatory Affairs: Pharmaceuticals,...

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices

John J. Tobin, Gary Walsh
你有多喜欢这本书?
下载文件的质量如何?
下载该书,以评价其质量
下载文件的质量如何?
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.
年:
2008
出版:
New
出版社:
Wiley-VCH
语言:
english
页:
298
ISBN 10:
3527318771
ISBN 13:
9783527318773
文件:
PDF, 7.32 MB
IPFS:
CID , CID Blake2b
english, 2008
线上阅读
正在转换
转换为 失败

关键词