Kamis, 29 November 2012

[V821.Ebook] Download PDF Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh

Download PDF Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh

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Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh

Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh



Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh

Download PDF Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh

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Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices, by John J. Tobin, Gary Walsh

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.

  • Sales Rank: #672392 in Books
  • Published on: 2008-09-02
  • Original language: English
  • Number of items: 1
  • Dimensions: 9.80" h x .85" w x 6.90" l, 1.55 pounds
  • Binding: Hardcover
  • 297 pages

Review
"This book is an excellent reference for people starting out in regulatory affairs, as well as those working within the area whose product portfolio is adapting and changing." (Microbiology Today, May 2009)

About the Author
J.J. Tobin worked for many years and in various capacities within Olympus diagnostica GmbH, a company employing several 100 people who develop and manufacture in vitro diagnostic reagents. Dr. Tobin therefore has extensive experience of working within an FDA and European medical device regulatory framework.

Gary Walsh is a senior lecturer in industrial biochemistry at the University of Limerick, Ireland. He has direct industrial experience within the pharmaceutical industry, as well as extensive teaching and non-laboratory based research interests in the pharmaceutical biotechnology arena. He has published a number of books, book chapters and journal articles relevant to this publication. He also teaches elements of pharmaceutical science and regulatory affairs on an annual course provided by the University of Limerick to an international medical device company with a manufactoring facility based in the region.

Most helpful customer reviews

1 of 1 people found the following review helpful.
good book
By Luciano O. Ferreira
written in a technically precise and easy-going manner, it covers well all items listed in the index. Allocation of tables and pictures sometimes far from the page one is reading, but no harm done. Overall it is an excellent book to align a team of RA professionals with the basics of the area.

See all 1 customer reviews...

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