Training Features
Person Responsible for Regulatory Compliance (PRRC) under the EU MDR and IVDR
A comprehensive virtual training on the responsibilities and requirements of the Person Responsible for Regulatory Compliance (PRRC) under the EU MDR and IVDR.
Format
Virtual Training
Level
Basic
Date
23 and 30 October 2025
Time
14:00 - 17:00 CEST
8:00 - 10:00 am EDT
Duration
6 hours in total
Trainer
René Schings
Exam
Exam and certificate included
Price
€ 1270 or equivalent currency
PRRC Training: Ensuring Compliance with EU MDR/IVDR Requirements
The Person Responsible for Regulatory Compliance (PRRC) is a key role introduced under the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). As a PRRC, you are accountable for ensuring compliance across all aspects of the device lifecycle, including technical documentation, quality management, clinical evidence, and post-market surveillance. Given these broad responsibilities, appropriate qualifications and experience are essential. This training provides in-depth knowledge of the PRRC role and supports a clear understanding of the MDR/IVDR requirements, from clinical evaluation to labelling.
Flexible Online PRRC Training Designed for Busy Professionals
Participate from anywhere with our interactive virtual format, designed to fit your schedule while delivering in-depth, actionable content tailored to real-world regulatory challenges.
Upon successful completion of the program, participants receive a recognized certification, boosting their career prospects and demonstrating their expertise to employers and clients.
Certification and Career Advancement
Learn directly from regulatory experts with hands-on industry experience, ensuring you gain practical insights and a clear understanding of the PRRC role under EU MDR and IVDR.
Expert-Led PRRC Training for Practical Compliance
Meet the Trainer
René Schings
René, with over 20 years of management experience in Quality Management, Research & Development, and more, serves as a lead auditor at Qserve, specializing in ISO audits, and brings expertise in building QMS for start-ups, managing complex change projects, and overseeing multi-site, multi-cultural teams, having previously held senior positions in the Medical Device and Consumer Electronics industries.
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