UNLIMITED FREE
ACCESS
TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

EU/EC - MEDDEV 2.7.1

EVALUATION OF CLINICAL DATA: A GUIDE FOR MANUFACTURERS AND NOTIFIFIED BODIES

inactive
Buy Now
Organization: EU/EC
Publication Date: 1 April 2003
Status: inactive
Page Count: 19

Document History

June 1, 2016
GUIDELINES ON MEDICAL DEVICES CLINICAL EVALUATION: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES UNDER DIRECTIVES 93/42/EEC and 90/385/EEC
A description is not available for this item.
December 1, 2009
GUIDELINES ON MEDICAL DEVICES CLINICAL EVALUATION: A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES
The primary purpose of this document is to provide manufacturers and notified bodies with guidance on how to conduct and document the clinical evaluation of a medical device as part of the conformity...
December 1, 2008
GUIDELINES ON MEDICAL DEVICES EVALUATION OF CLINICAL DATA - A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES - Appendix 1 : Clinical Evaluation of Coronary Stents
A description is not available for this item.
MEDDEV 2.7.1
April 1, 2003
EVALUATION OF CLINICAL DATA: A GUIDE FOR MANUFACTURERS AND NOTIFIFIED BODIES
A description is not available for this item.
Advertisement