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Picture Of Tom Melvin
Tom Melvin
Course Time 22 Min

Competent Authority Expectations and Management of Device Clinical Study Applications Under the MDR

VOD
About the Course
Picture Of Maria Donawa
Maria Donawa
Course Time 29 Min

Aligning Clinical Investigations and Risk Management to Ensure MDR Compliance

VOD
About the Course
Picture Of Maria Donawa
Maria Donawa
Course Time 45 Min

MDR Requirements for Sponsor GCP Inspections (audits) and How to Conduct Them

VOD
About the Course
Picture Of Nils-Åke Lindberg
Nils-Åke Lindberg
Course Time 29 Min

Standards, Harmonisation Process and Common Specifications

VOD
About the Course
Picture Of Claire Murphy
Claire Murphy
Course Time 29 Min

General Safety and Performance Requirements under the Medical Devices

VOD
About the Course
Picture Of Robert Ginsberg
Robert Ginsberg
Course Time 27 Min

Software, Artificial Intelligence and Cybersecurity in the European Union

VOD
About the Course
Picture Of Maurizio Suppo
Maurizio Suppo
Course Time 28 Min

Issues Arising from the Implementation of the IVD-Regulations

VOD
About the Course
Picture Of Helene Quie
Helene Quie
Course Time 33 Min

Clinical Evaluation, Investigations and PMCF under MDR

VOD
About the Course
Picture Of Mindy Mc Caan
Mindy Mc Caan
Course Time 29 Min

Major Regulatory Compliance Challenges for the Non-European Industry

VOD
About the Course
Picture Of Helene Quie
Helene Quie
Course Time 18 Min

Benefit Risk Assessment

VOD
About the Course

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