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Highlights

June 27, 2022 - June 27, 2022 / Europe

Clinical Suite | Clinical Evaluation under the MDR

CE Certification Clinical Evaluation Market Access Europe MDR 2017/745 Medical Device Regulations Training

June 30, 2022 - July 07, 2022 / Europe

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

CE Approved CE Certification CE Registration Market Access Europe MDR 2017/745 Medical Device Regulations PRRC Regulatory Compliance Training

Results

May 31, 2022 - May 31, 2022 / Europe

Meet and Greet with Gert Bos at the MDR symposium hosted by NEN

Medical Device Regulations MedTech

June 02, 2022 - June 03, 2022 / Europe

(Virtual) Meet and Greet with Coenraad Davidsdochter at the Medical Device Safety And Regulations Compliance Forum by GlobalBSG

Artificial Intelligence Conference Medical Device Regulations

June 20, 2022 - June 24, 2022 / Europe

Meet and Greet with Gert Bos at the Medtech Summit 2022: The Flagship Regulatory Event of the Year hosted by Informa Connect

Medical Device Regulations MedTech

June 21, 2022 - June 21, 2022 / Europe

Free Webinar | Effectively Managing Clinical Data Collection Using Cost-Sensitive Methods – PMCF Surveys

CE Certification CE Registration Clinical Affairs Clinical Data Clinical Evidence Clinical Investigation Clinical Surveys Market Access Europe MDR 2017/745 Medical Device Regulations PMCF Post Market Clinical Follow-up Regulatory Affairs

June 23, 2022 - June 23, 2022 / Europe

Free Webinar | UK market access: UKCA challenges in uncertain times

UK Responsible Person UKCA

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