The European MEDDEV 2.12.1 entitled "Guidelines on a Medical Devices Vigilance System" has been revised. Revision 6 includes minor “technical” modifications to the Incident Report Form, Annex 3. This has been revised to include the following:
The link to MEDDEV 2.12.1, REV 5 on the European Commission web site no longer functions. However, you can find and download the latest PDF version of MEDDEV 2.12-1 REV 6 in our Learning Library here: http://www.emergogroup.com/resources/regulations-europe
There are also new references published in the Official Journal of European Communities for standards harmonized to the medical devices directives. The revised Annex 3 will be applicable starting 20 March 2010.