MDR Person Responsible for Regulatory Compliance

Article 15 of the Medical Device Regulations (EU 2017/745) states that a company must employ someone who has the appropriate expertise to act as the Person Responsible for Regulatory Compliance (PRRC). In a small or micro organisation, the role of the PRRC may be subcontracted out to an external party. The PRRC is responsible for ensuring all regulatory activities are undertaken at all times. Cranage Veritas have the expertise to be able to offer a PRRC service to small or micro organisations. Get in touch with our team today to discuss your MDR (EU 2017/745) requirements.

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