Aktuelle Revision der Medizinprodukte-Richtlinien

The European Commission is currently in the revision process of the Medical Devices Directive (MDD) and will comply with the efforts to tighten by a transparent cooperation with the Member...

Industrial, Technology

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The European Commission is currently in the revision process of the Medical Devices Directive (MDD) and will comply with the efforts to tighten by a transparent cooperation with the Member States' checks, ensure the safety of medical devices to better and the patient's confidence in the relevant legislation and its to strengthen implementation. Which changes must adjust the medical device industry and how the current state of the review process looks like - here provide information leading experts from industry, authorities, Notified Body and Health. We invite you over for a first experience in which you information many stringent regulatory requirements, obtain the extension of the scope and their impact on corporate practices, monitoring and market development. You will also receive guidance and tips for putting it into practice and into your business strategy and can be used in intensive discussion with the speakers to find out important details

When
From: September 20, 2012 00:00
To: September 20, 2012 23:59
Where

Sheraton Offenbach, Berliner Str 111, 63065, Frankfurt, Germany

Category

Industrial, Technology

Tags

business, development, medical devices

Hashtag

#AkademieHD

Contact email
info@akademie-heidelberg.de

Website

Submitted by:

Conrad

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