Regulatory Affairs for Biomaterials and Medical Devices



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Éditeur :

Woodhead Publishing


Paru le : 2014-10-27



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Description
All biomaterials and medical devices are subject to a long list of regulatory practises and policies which must be adhered to in order to receive clearance. This book provides readers with information on the systems in place in the USA and the rest of the world. Chapters focus on a series of procedures and policies including topics such as commercialization, clinical development, general good practise manufacturing and post market surveillance. - Addresses global regulations and regulatory issues surrounding biomaterials and medical devices - Especially useful for smaller companies who may not employ a full time vigilance professional - Focuses on procedures and policies including risk management, intellectual protection, marketing authorisation, university patent licenses and general good practise manufacturing
Pages
202 pages
Collection
n.c
Parution
2014-10-27
Marque
Woodhead Publishing
EAN papier
9780857095428
EAN PDF
9780857099204

Informations sur l'ebook
Nombre pages copiables
20
Nombre pages imprimables
20
Taille du fichier
4516 Ko
Prix
174,07 €
EAN EPUB SANS DRM
9780857099204

Prix
174,07 €

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