With the medical regulatory landscape having undergone its most significant overhaul in years comes a need to stay up-to-date with the latest regulatory intelligence and how the changes might impact your organization. LRQA has developed a series of webinars to discuss the current state of the regulations.
IVDR Overview – LIVE on January 26, 2017 at 10:00 am CST - REGISTER NOW!
Join this live webinar for an opportunity to ask IVD experts questions as they discuss an overview of changes and priorities initiated by the new IVDR requirements including:
- EU Referendum
- Negotiations – latest state of play
- What’s new? Key changes in IVDR from current Directives
- Implementation – Timescale & Challenges
MDR Overview (On Demand)
Experts from LRQA discuss the current status of the new MDR Regulation, the transition period for manufacturers and the expected 'Entry into Force' of the regulation. A comprehensive overview of the key changes which will affect all Medical Device manufacturers as well as the priorities for the different authorities will also be reviewed.
ISO 13485:2016 – Understanding Risk Management Implications (On Demand)
In this 20 minute webcast, Susan Mecca, Senior Technical Manager, Medical Devices - LRQA Americas, will provide practical guidance and real-world application and implementation of some of the new additions and revisions in ISO 13485:2016, particularly those around Risk Management and the Interconnection with other Regulatory Requirements to the corresponding Medical Device Directives (MDD) and In Vitro Diagnostic Medical Devices (IVDD).