[Webinar] Preparing your QMS for EU MDR
Updated: Mar 6
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 email@example.com if you have any questions.