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If you think you have a talk or content that you'd like to share with our audience, then we'd love to hear from you.

Effective Post-market Surveillance in the EU under MDR March 16, 2021, 04:00 PM
Isabella Schmitt Director of Regulatory Affairs, Proxima Clinical Research
Risk Management According to EU MDR or ISO 14971? March 17, 2021, 03:00 PM
Peter Sebelius Founder, Medical Device HQ
How to Prepare for Common MDR Audit Pitfalls March 18, 2021, 01:00 PM
Bassil Akra CEO & Co-Owner, QUNIQUE GmbH
Prepare Now for the EUDAMED UDI/Registration Module March 15, 2021, 04:00 PM
John Lorenc & Gary Saner Reed Tech & Reed Tech

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