The QMS Update - Part 2

 

New QMS video series

 

We have launched our new QMS video series today.  This 6 part series will concentrate on:-

  • why medical device manufacturers need a QMS

  • the importance of ISO 13485

  • the structure of ISO 13485

  • helpful tools eg - eQMS

  • the importance of change control/CAPA

 

Visit our website to watch the first video: https://www.psephos.com/quality-management-services.

 

The strategic implementation of the right QMS at the right time for your Medtech venture is what Psephos offers, from concept to commercialisation and beyond. Contact us below to discuss your QMS.

EU MDR and ISO 13485:2021

 
An EN ISO 13485 compliant QMS helps manufacturers align their processes with the EU MDR requirements. The 2021 version specifically provides guidance on meeting the EU MDR. Are you currently using ISO 13485:2021 to show compliance to the EU MDR? If not, we can help you with this process. Get in touch with us to find out how.

CompanionQMS

 
We are proud to partner with CompanionQMS to provide a quickly deployed, user-friendly and adaptable electronic QMS. Frank Enright of CompanionQMS will be joining us at the SEHTA 2023 Medtech Conference on Friday 3rd November. Come and have a chat with Frank and the Psephos team at our stand.

 

https://sehta.co.uk/Events/SEHTA-2023-MedTech-Expo/

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