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重点
培训
六月 27, 2022 - 六月 27, 2022 /
Clinical Suite | Clinical Evaluation under the MDR
标签
CE Certification
Clinical Evaluation
Market Access Europe
MDR 2017/745
Medical Device Regulations
Training
培训
六月 30, 2022 - 七月 07, 2022 /
Virtual Training: PRRC | Person Responsible for Regulatory Compliance
标签
CE Approved
CE Certification
CE Registration
Market Access Europe
MDR 2017/745
Medical Device Regulations
PRRC
Regulatory Compliance
Training
结果
活动
五月 31, 2022 - 五月 31, 2022 /
Meet and Greet with Gert Bos at the MDR symposium hosted by NEN
标签
Medical Device Regulations
MedTech
活动
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
标签
Artificial Intelligence
Conference
Medical Device Regulations
活动
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
标签
Medical Device Regulations
MedTech
网络课程
六月 21, 2022 - 六月 21, 2022 /
Free Webinar | Effectively Managing Clinical Data Collection Using Cost-Sensitive Methods – PMCF Surveys
标签
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
网络课程
六月 23, 2022 - 六月 23, 2022 /
Free Webinar | UK market access: UKCA challenges in uncertain times
标签
UK Responsible Person
UKCA
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