Person Responsible for Regulatory Compliance (PRRC) Training

Comply Guru are the first in the world to offer RAPS Certified Person Responsible for Regulatory Compliance (PRRC) Training offering a credential for the Medical Device Industry that is globally recognized.

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EU MDR EU IVDR PRRC Medical Devices

Person Responsible for Regulatory Compliance (PRRC) Training

6hrs
RAPS Certified Course

Person Responsible for Regulatory Compliance (PRRC) Training provides clarity on the role and responsibilities of the PRRC introduced under Article 15 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR).

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2026 Training Guide

Transformational Training for ISO Standards, Auditing & Medtech QA/RA

2026 Training Guide

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Our team has you covered with expert insights & updates to stay on top of the latest updates, trends, and changes in the industry.

Design Controls, Design and Development under FDA QMSR
Michelle discusses Design Controls, ISO 13485 Design and Development and what endures under the FDA's QMSR in effect from February 2026....
Reaffirmed, Not Static: ISO 13485 and the Global Regulatory Evolution
Michelle discusses the recent affirmation of ISO 13485:2016 and shares her insights on the new guidance reflecting a Global Regulatory Evolution....
Low Risk Does Not Mean No Risk
Michelle discusses why ISO 13485 and ISO 14971 make a critical clarification on Risk, and clarifies a dangerous misconception in medical device develo...