Training Services
Empowering Your Team with Regulatory Expertise
Keeping your team informed and qualified is critical for maintaining compliance in the fast-evolving medical device sector. EUCEREP offers specialized training programs designed to equip professionals with the knowledge and skills needed to navigate EU and UK regulations confidently.
ISO 13485 Lead
Auditor Training
In partnership with PECB, EUCEREP delivers ISO 13485 Lead Auditor courses designed for professionals who conduct and lead audits of medical device Quality Management Systems. This comprehensive training covers audit principles, regulatory requirements, and practical auditing techniques aligned with the ISO 13485:2016 standard.
Certified PRRC
Training
EUCEREP offers CPD-accredited training for individuals aiming to fulfill the role of Person Responsible for Regulatory Compliance (PRRC) under the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). This program prepares participants to manage regulatory obligations effectively and ensure ongoing compliance.
