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Medical Device Regulatory Practices

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Medical Device Regulatory Practices

0 - Default Title
Description
This book is intended to serve as a reference for professionals in the medical device industry, in particular those seeking to learn from practical examples and case studies. Medical devices, like pharmaceuticals, are highly regulated and the bar is raised constantly as patients and consumers expect the best quality healthcare and safe and effective medical technologies. Most books on regulatory affairs present regulations in each jurisdiction separately: European Union, USA, Australia, Canada, and Japan. This book proposes practical solutions for a coherent, one-size-fits-all (or most) set of systems and processes in compliance with regulations in all key markets.
Product details
Edition:
1
Number of Pages:
592
Release Date:
2015-08-03
Publication Date:
2015-08-03
Publisher:
Jenny Stanford Publishing
Languages:
Original: English
ISBN10:
9814669105
ISBN13:
9789814669108
GPSR Manufacturer Reference:
Weight:
997 g
Height:
157 cm
Width:
235 cm
Thickness:
36 cm
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