Moscow, Russia
General updates
Presentation: Improving the quality of international medical device standards for regulatory use
Presentation: How the Guidance Supports the Goals of Regulatory Harmonization
Presentation: Guidance Structure and Key Proposal
Presentation: How standards are used for regulatory purposes among IMDRF members
Presentation: Optimized standards to support essential principles of safety and performance of medical devices
Presentation: How IEC can contribute to IMDRF to support regulatory convergence
Presentation: Test methods in standards requirements and proposals
Presentation: How new work items come to be Good standards development practice
Presentation: SWG Optimizing Standards for Regulatory Use
Presentation: Use of improved Standards from the Russian industry perspective
Presentation: Why standards that follow the guidance are good for business
Presentation: Future of ISO 13485 and update on ISO 14971
Presentation: The future of the IEC 60601 SERIES
Presentation: Optimizing Standards for Regulatory Use_keynote summary
Presentation: FDA Overview on NGS Testing
Presentation: Next Generation Sequencing
Presentation: NGS Dx & EU Regulation
Presentation: NGS First Genetics
IMDRF Presentation - Stakeholder - AHWP Update
IMDRF Presentation - Stakeholder - APEC Update
IMDRF Presentation - Stakeholder - DITTA Update
IMDRF Presentation - Stakeholder - EAEC Update
IMDRF Presentation - Stakeholder - GMTA Update
IMDRF Presentation - Stakeholder - IAMT Update
IMDRF Presentation - Stakeholder - IMEDA Update
IMDRF Presentation - Stakeholder - PAHO Update
IMDRF Presentation - Stakeholder - WHO Update
Jurisdictional updates
Australia
Brazil
Canada
China
Japan
Russia
Singapore
South Korea
Working group updates
Adverse Event Terminology
Good Regulatory Review Practices
Medical Device Clinical Evaluation
Medical Device Cybersecurity
Personolized Medical Devices
Regulated Products Submission
Standards
Unique Device Identification