© 2017 Rook Quality Systems. All Rights Reserved. 

[Webinar] Preparing your QMS for EU MDR

May 3, 2019

This webinar was hosted by Kyle Rose, President of Rook Quality Systems.


You will find this webinar helpful for understanding how Rook helps companies identify the critical steps needed to prepare your QMS for the upcoming EU Medical Device Regulations in 2020. 


The in-depth webinar will cover some of the most important action items that must be taken ASAP by companies. 

  • Updates to Compliant Handling and Vigilance 

  • Documentation and requirements for each category of Economic Operators within the supply chain 

  • Updates to comply with SPRs 

  • Incorporating UDI and EUDAMED into your labeling and traceability SOPs 

  • Procedures for the regulatory compliance strategy 

  • New requirements for Implantable devices  


Please contact us at info@rookqualitysystems.com if you have any questions. 



Sponsored by 







Share on Facebook
Share on Twitter
Please reload

Recent Posts
Please reload

Please reload

Search By Tags