NitroFlare Medical Product Regulatory Affairs Pharmaceuticals, Diagnostics, Medical Devices

Discussion in 'E-Books & Tutorials' started by kocogi, Aug 28, 2015.

  1. kocogi

    kocogi Active Member

    Joined:
    May 29, 2012
    Messages:
    17,043
    Likes Received:
    12
    Trophy Points:
    38
    [​IMG]

    John J. Tobin, Gary Walsh, "Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices"
    2008 | ISBN-10: 3527318771 | 297 pages | PDF | 7 MB


    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.[​IMG]
    Buy Premium From My Links To Get Resumable Support,Max Speed & Support Me
    Code:
    Download ( NitroFlare )
    http://nitroflare.com/view/C41B9C0CB19C9A3/hsx4r.Medical.Product.Regulatory.Affairs.Pharmaceuticals.Diagnostics.Medical.Devices.Repost.rar
    
    
    
    
    
    
    
    
    
     

Share This Page