EUDAMED ACTOR MODULE FAQs – update

By Published On: January 3rd, 20220.4 min read
Categories: Compliance, Regulatory

EUDAMED ACTOR MODULE FAQs – update

By Published On: January 3rd, 20220.4 min read
Categories: Compliance, Regulatory

The European Commission has updated the Eudamed Actor Module FAQs.

The document includes a revision of paragraph 4.6.4 relating to the publicly accessible contact details of Person Responsible for Regulatory Compliance (PRRC).
Read more in the EC document.

Contact Meditrial for immediate assistance in Europe and in the US.

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This article provides general information and does not constitute regulatory, legal, clinical, or compliance advice. Requirements and appropriate processes may vary by study, product, jurisdiction, and organization. Medigen Suite functionality should be used in accordance with applicable regulations, study documentation, and internal procedures.

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