The Person Responsible for Regulatory Compliance (PRRC) is a requirement of the Medical Device Regulation (MDR) and In-Vitro Diagnostic Regulation (IVDR). Medical Device and IVD professionals across the globe are taking on this responsibility for their organisation.

• But what does it mean if you are the PRRC for your company?
• What happens if things do not go to plan? Are you responsible?
• Are you experienced or qualified enough to take on the role?
• What should you do now to plan and prepare for the role? 

 

We discussed the role with our Educo Life Science trainer Anne Jury. Anne is the Vice President of Team-PRRC. Their aim is to create a support network for professionals in PRRC roles. 

 

Watch the full interview below…….

Anne teaches the following courses:

PRRC Training (Person Responsible for Regulatory Compliance)

Overview of Regulatory Affairs for Medical Devices

 

View all our Medical Device and IVD courses:

View our courses here