Newly adopted EC regulation EU 207/2012 will introduce a new electronic labeling requirement for medical devices on the European market.
Newly adopted EC regulation EU 207/2012 will introduce a new electronic labeling requirement for medical devices on the European market.
Ireland's 2013 EU presidency to set increased focus on requirements for notified bodies, medical device manufacturers, and authorized representatives.
More information on the previously missing EU standards EN 980 and EN ISO 15223-1. The Commission's intention was to have EN ISO 15225-1 replace EN 980.
The European Association of Notified Bodies for Medical Devices have published a paper questioning the auditing process for Authorized Representatives.
The new EU regulation for medical devices comes into force in August 2012. It contains a number of changes for devices containing tissue of animal origin.
Further reading on the European Commission's press conference on proposed changes to European medical and in-vitro diagnostic device legislation.
European Commission has released a new list of harmonized standards for medical devices on the European market. Learn more about the new important updates.
New changes have been made to directive 76/768/EEC annexes to allow for new knowledge and practices in hair dying products, formulation, and notification.
The updated Waste Electrical & Electronic Equipment directive places new obligations on medical devices in the EU. Find out how to reach compliance with Obelis.
A new EU Commission recommendation, in line with 2006/647/EC) mandates the standardization of claims and labelling for sunscreen products on the EU market.