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重点

九月 16, 2020 - 九月 17, 2020 /

Open Training: Update on the New ISO 14155:2020 - GCP

CE Certification Contract Research Organization CRO Europe GCP ISO14155 GCP Training

九月 17, 2020 - 九月 24, 2020 /

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

Medical Device Regulations Medical Devices MedTech PRRC Regulatory Affairs Regulatory Compliance Training

结果

八月 20, 2020 - 八月 21, 2020 /

Meet and Greet mit Stefan Menzl beim Workshop MDR Compliance von Innovald

Medical Device Regulations MedTech

九月 08, 2020 - 九月 08, 2020 /

Free Webinar: How the MDR Impacts the QMS? Beyond the Obvious Aspects We Already Know.

Clinical Affairs Clinical Evaluation PMCF PMCF Requirements QMS Regulatory Affairs Risk Management

九月 16, 2020 - 九月 17, 2020 /

Open Training: Update on the New ISO 14155:2020 - GCP

CE Certification Contract Research Organization CRO Europe GCP ISO14155 GCP Training

九月 17, 2020 - 九月 24, 2020 /

Virtual Training: PRRC | Person Responsible for Regulatory Compliance

Medical Device Regulations Medical Devices MedTech PRRC Regulatory Affairs Regulatory Compliance Training

九月 28, 2020 - 九月 29, 2020 /

IVDR Fundamentals | What You Need to Know Before You Start Implementation

Clinical Evaluation Clinical Evidence Clinical Investigation In-Vitro Diagnostics IVDR

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