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活动和培训

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六月 27, 2022 - 六月 27, 2022 /

Clinical Suite | Clinical Evaluation under the MDR

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

六月 30, 2022 - 七月 07, 2022 /

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

结果

五月 31, 2022 - 五月 31, 2022 /

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

Medical Device Regulations MedTech

六月 02, 2022 - 六月 03, 2022 /

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

Artificial Intelligence Conference Medical Device Regulations

六月 20, 2022 - 六月 24, 2022 /

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

六月 21, 2022 - 六月 21, 2022 /

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 Regulatory Affairs

六月 23, 2022 - 六月 23, 2022 /

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

UK Responsible Person UKCA

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