Critical Considerations in Site Selection and Subject Enrollment in Device and IVD Clinical Studies
Matteo Mosso
Donawa Lifescience, Italy
Free
Developing Clinical Investigation and Performance Study Plans That Meet Regulatory and Operational Requirements
Daniela Karrer
Donawa Lifescience, Italy
Free
Aligning Clinical Investigations and Risk Management to Ensure MDR Compliance
Maria Donawa
Member of the Board, EAAR,…
Free
MDR Requirements for Sponsor GCP Inspections (audits) and How to Conduct Them
Maria Donawa
Member of the Board, EAAR,…
Free
Standards, Harmonisation Process and Common Specifications
Nils-Ã…ke Lindberg
Member of the Board, EAAR;…
Free
General Safety and Performance Requirements under the Medical Devices
Claire Murphy
EAAR Member of the Board,…
Free
Software, Artificial Intelligence and Cybersecurity in the European Union
Robert Ginsberg
EAAR Member of the Board,…
Free
Benefit Risk Assessment
Helene Quie
Member of the Board, EAAR,…
Free