EU MD Regulation : the race to compliance

In a survey published by KPMG and the RASP (Regulatory Affairs Professional Society), more than 200 Quality and Regulatory Affairs managers were asked how prepared they feel regarding the coming EU MD Regulation. The companies that took part in the s...

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MD additive manufacturing : FDA guidance

The FDA published on December 5th the final issue of the guidance document "Technical Considerations for Additive Manufactured Medical Devices", dedicated to manufacturers intending to exploit this new process. This 31 pages document details th...

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Askorn at Medtec Ireland

Askorn is attending the Medtec event in Galway, Ireland, the 4th and 5th of October at the Radisson Blu Hotel. Medtec brings together over 900 Medical Device professionals from various countries around the world. The exhibition serves not only ...

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Team NB : 2016 survey results

On May 9, 2017, the European Association for Medical Devices of Notified Bodies Team-NB published the results of its yearly survey run among its 21 members, in order to collect data on certificate emission and analyse the variation with previous yea...

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