(Re)Watch our Regulatory Compliance Webinars

Explore the Ackomas ecosystem through our exclusive webinar series focused on EUDAMED, GUDID, MDR, IVDR, and digital regulatory transformation. This page gathers all our expert-led sessions designed to guide you from compliance preparation to full implementation.

Webinar Replays & Resources – Free Access

Missed a session or want to dive deeper? Access all past webinars on-demand, along with downloadable slides and supporting materials. Learn from real-world examples, gain expert insights, and strengthen your readiness for audits and regulatory reporting.

EUDAMED & GUDID regulatory alerts — delivered to your inbox

Receive concise updates on MDR/IVDR regulatory changes, EUDAMED registration deadlines, and GUDID compliance requirements. Built for RA/QA and regulatory affairs teams. No promotional content — only actionable changes.

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A smartphone displaying an email about an EU medical regulation update rests on a table next to eyeglasses, a printed regulatory timeline, and a cup of coffee.
  • Webinar replays & regulatory briefings

    Watch recorded sessions on EUDAMED registration, UDI structuring, and data governance

  • Deadline alerts & regulatory changes

    Be notified when EUDAMED deadlines, MDCG guidance, or submission rules change

  • Compliance guidance for your team

    Practical resources to prepare for audits, structure your UDI data, and manage multi-market registration