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.

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.
Learn more with Obelis about the impact the new medical and in-vitro device regulation proposals may have for Authorized Representatives within the EU.
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.
In April 2012, the National Agency for the Safety of Medicines and Health Products will replace current medical device regulatory agency, Afssaps, in France.
The updated Waste Electrical & Electronic Equipment directive places new obligations on medical devices in the EU. Find out how to reach compliance with Obelis.
The proposed new EU medicines and medical device vigilance portal – EUDAMED – aims to increase oversight and incident reporting systems throughout Europe.
The 3rd edition revision of IEC 60601-1 for medical devices in Europe will come into effect in June 2012. Learn more about EU harmonized standards with Obelis.