Global Regulatory Affairs | Services
Have a look at the slides to see how Asphalion´s expertise can help you with your regulatory
September 6, 2023
Have a look at the slides to see how Asphalion´s expertise can help you with your regulatory
A lot of things have happened during these past three months. We received an award from AEFI
El Ministerio de Sanidad ha publicado oficialmente la nueva Orden por la que se regulan determinados aspectos
Asphalion’s Managing Director, Núria Romero, and Lidia Cánovas, Key Accounts Director will be joining the Medicines for
Article 86 MDR requires manufacturers of Class IIa, Class IIb, and Class III devices to prepare a Periodic Safety Update Report (PSUR) for each device and, when relevant, for each category or group of devices. The MDCG 2022-21 guideline endorsed by the Medical Device Coordination Group (MDCG) provides ideas for manufacturers on how to prepare the PSUR for their Medical Devices.
At Asphalion we are always up to date with the latest digital developments! This is why our
This practical seminar is aimed at anyone
involved in planning, creating or submitting
variations.
Asphalion has been featured as one of the 10 Best Healthcare Solution Companies in 2022.
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