No grandfathering is going to be valid at this time?

Are you ready for implementing the changes? All devices in the market must be compliant with the new Regulations at the end of the transition period.

May 5, 2017

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No grandfathering is going to be valid at this time? Are you ready for implementing the changes?

All devices in the market must be compliant with the new Regulations at the end of the transition period.

A conformity assessment will be needed for all existing and new medical devices.

It is time to review and start implementation plans!

Keep following us and be updated on all changes and implementation plans, contact us for specific questions or implementation plans if desired.

Get ready for the upcoming changes! We are organizing an on-line webinar to assist you about their implementation.

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Brexit updates for human use medicinal products approved via MRP/DCP

December 21, 2020

As Brexit is quickly coming closer, the CMDh has published an updated version of the Practical guidance for procedures related to Brexit for medicinal products for human use approved via MRP/DCP in December 2020.

Javier Febrero Alija – New Regulatory Information Manager

December 17, 2020

Asphalion is excited and proud to officially welcome Javier Febrero Alija to its team as Regulatory Information Manager, expert in Data Management and RIMS.

Season’s Greetings

December 17, 2020

We wish you Happy ‘Xmas, Prosperous New Year and Health for you and your loved ones.

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No grandfathering is going to be valid at this time?

Are you ready for implementing the changes? All devices in the market must be compliant with the new Regulations at the end of the transition period.

Search

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Related news and events

Brexit updates for human use medicinal products approved via MRP/DCP

Javier Febrero Alija – New Regulatory Information Manager

Season’s Greetings

About

Team

Partners

CSR

AI Ethic Code

Careers

No grandfathering is going to be valid at this time?

Are you ready for implementing the changes? All devices in the market must be compliant with the new Regulations at the end of the transition period.

Search

Filter by category

Related news and events

Brexit updates for human use medicinal products approved via MRP/DCP

Javier Febrero Alija – New Regulatory Information Manager

Season’s Greetings

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