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A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

Regulatory updates on the standard 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.

February 4, 2013
Marketing 2013-02-04T14:13:00+01:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

How and whether to Audit Authorized Representatives?

The European Association of Notified Bodies for Medical Devices have published a paper questioning the auditing process for Authorized Representatives.

January 10, 2013
Marketing 2013-01-10T16:55:00+01:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

Impact on the Authorized Representative by NEW medical device proposals

Learn more with Obelis about the impact the new medical and in-vitro device regulation proposals may have for Authorized Representatives within the EU.

October 11, 2012
Marketing 2012-10-11T13:14:00+02:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

The EU Regulation 722/2012 on utilizing tissues of animal origin

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.

October 9, 2012
Marketing 2012-10-09T13:20:00+02:00
Natural cosmetic products photoshoot
Beauty and personal care, Medical devices and healthcare, Medical devices and healthcare auto

Review of Press Conference on NEW Proposals of European Medical Device Legislation

Further reading on the European Commission's press conference on proposed changes to European medical and in-vitro diagnostic device legislation.

October 2, 2012
Marketing 2012-10-02T13:18:00+02:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

New lists of harmonized standards for medical devices published by EU Commission

European Commission has released a new list of harmonized standards for medical devices on the European market. Learn more about the new important updates.

September 10, 2012
Marketing 2012-09-10T13:26:00+02:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

New Agency for Medical Device Registration in France

In April 2012, the National Agency for the Safety of Medicines and Health Products will replace current medical device regulatory agency, Afssaps, in France.

July 19, 2012
Marketing 2012-07-19T18:10:00+02:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

New WEEE Directive’s Affects on Medical Devices

The updated Waste Electrical & Electronic Equipment directive places new obligations on medical devices in the EU. Find out how to reach compliance with Obelis.

July 2, 2012
Marketing 2012-07-02T13:25:00+02:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

Early Implementation of an EU Vigilance Portal

The proposed new EU medicines and medical device vigilance portal – EUDAMED – aims to increase oversight and incident reporting systems throughout Europe.

May 14, 2012
Marketing 2012-05-14T11:47:00+02:00
A professional uses an ultrasound machine
Medical devices and healthcare, Medical devices and healthcare auto

Revision of the IEC 60601-1 Regarding Medical Devices, 3rd Edition

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.

May 8, 2012
Marketing 2012-05-08T13:28:00+02:00

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