The New European Medical Device Regulation – A comprehensive overview in questions and answers. View larger

MEDICAL DEVICE REGULATION

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New product

Date of publishing June 19, 2017

COMPENDIUM
THE NEW EUROPEAN

MEDICAL DEVICE REGULATION

A comprehensive overview in questions and answers.
By Daniel Shoukier | BellingsBooks Publishing House

For Business customers and bookshops:
Orders please via bestellung@bellingsbooks.com
or phone +41 (0)79 429 1590.

ISBN 978-3-9523794-1-7 | Price in EUR: 64.00

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200 Items

64.00 CHF

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Book qualitySoftcover
LanguageEnglisch

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This compendium is a quick overview of the new MDR and is intended to give the interested reader an easier access to the complex subject matter. The compendium is predominantly designed as a question-and-answer text and deals with the most important aspects of the medical device regulation.

ABOUT THE AUTHOR

Daniel Shoukier is a worldwide-recognized regulatory expert for medical devices and a book author of several publications. He is the Managing Director of the Bellingswood Group, a consulting company for global market access and registration of medical devices and drug combination products. He is also a lead auditor and medical expert for a Swiss notified body. As a lecturer for professional academies he provides his student a deep understanding into the complex world of medical device regulation.

In the past, Daniel was the Vice President at Novo Nordisk, heading up Regulatory Affairs for medical devices. Before this he was the Global Director for regulatory affairs at Biosensors and Olympus Medical. He also worked in the past as a lead auditor at TÜV Rheinland.