Nice, France
Uncategorized
IMDRF Presentation - GHTF to IMDRF What's next?
IMDRF Presentation - Regulatory convergence WHO's perspective
IMDRF Presentation - International Regulatory Convergence: Challenges of the Global Health System
IMDRF Presentation - International Regulatory Convergence: Meeting Patients' Needs
IMDRF Presentation - International Regulatory Convergence: strategic reflections from the ESC
IMDRF Presentation - AHWP - IMDRF Articulation Towards Regulatory Convergence
IMDRF Presentation - DITTA - IMDRF Stakeholders Meeting
IMDRF Presentation - Definition and regulation in terms of mechanism of action and intended use
IMDRF Presentation - Regulatory guidance for validation and approval of standardized apheresis connectors
IMDRF Presentation - IMDRF RPS ToC WG Update
IMDRF Presentation - IMDRF RPS Update
IMDRF Presentation - IMDRF Project: List of international standards recognized by IMDRF management committee members
IMDRF Presentation - Medical Device Single Audit Program (MDSAP) Working Group
IMDRF Presentation - Unique Device Identification for medical devices and in vitro diagnostics medical devices
IMDRF Presentation - Review of the NCAR Exchange Program
IMDRF Presentation - China: Update on jurisdictional regulatory developments
IMDRF Presentation - Update on the Brazilian regulatory aspects on medical devices
IMDRF Presentation - Revision of the EU legislation on medical devices and in vitro diagnostic medical devices