we run Seminar on the Person Responsible for Regulatory Compliance (PRRC) which will be delivered in English with a live Q&A session at the end of the Seminar.

Two-day of comprehensive seminar which aims to provide initial knowledge and concepts for those interested in understanding and performing the role of Person Responsible for Regulatory Compliance (PRRC), (presentations are pre-recorded).

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The seminar is delivered by top industry experts who will review the regulation of medical devices in Europe (MDR/IVDR).

Seminar Topics:

  • Review of the new regulations of the European Medical Equipment Regulation (MDR / IVDR)

  • The role and duties of a PRRC.

  • Qualifications and experience of the PRRC

  • CE marking

  • Quality management system

  • Risk management and notified bodies

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Who is this seminar for?​

  • Medical equipment manufacturers

  • The team responsible for the regulation in the organization

  • RA manager, RA director, QA manager, QA director

₪1500

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