Making MedTech Happen with RQM+

Por: RQM+
RQM+ is The MedTech CRO – a full-service partner supporting everything from groundbreaking innovation to well-established technologies. Our coordinated and comprehensive solutions are customized to each client’s product and life cycle stage. By aligning strategy and execution in one partner, we help reduce cost, accelerate timelines, and drive more successful outcomes.

Visit RQMplus.com to see how we help MedTech companies of all sizes, spanning all device types and therapeutic areas.

This podcast provides audio/video we also share on our website and LinkedIn page. Thank you for listening!
197 episodios disponibles

Latest episodes of the podcast Making MedTech Happen with RQM+

Mostrando página 8 de 10

Live! #58 –Regulatory Landscape of Companion Diagnostics (CDx) in the EU 15/07/2022
Live! #57 – FDA Appeals Process (featuring panelists from Linear Health and DuVal & Associates, PA) 30/06/2022
Live! #56 – IVDR: A Notified Body Perspective (featuring Marta Carnielli of TÜV SÜD) 13/06/2022
Live! #55 – Is your labeling thrice as big as your device yet? 24/05/2022
Live! #54 – Implications of FDA Adopting ISO 13485 and How to Prepare 24/05/2022
Live! #53 – Part 2: PSURs – Ready, Set, Go! 26/04/2022
Live! #52 – Part 2: What’s new in the world of biocompatibility for medical devices? 11/04/2022
Live! #51 – Leveraging your medical directors and clinicians for successful regulatory submissions 29/03/2022
Live! #50 – IVDR Notified Body Application Process 14/03/2022
RQM+ Live! #49 — PSURs – Ready, Set, Go! 01/03/2022
RQM+ Live! #48 — Part 2: Sustaining EU MDR and IVDR certification in the post-market phase - What will it take? 15/02/2022
RQM+ Live! #47 — Have we been looking at EU MDR equivalence requirements all wrong? 31/01/2022
RQM+ Live! #46 — Year-end Review and 2022 Outlook on FDA Submissions 18/01/2022
RQM+ Live! #45 — What’s new in the world of biocompatibility for medical devices? 06/01/2022
RQM+ Live! #44 — Success Stories of PMCF Surveys: Strategy and Execution 03/12/2021
RQM+ Live! #43 — Spinal Implantable Device Classification Changes Resulting from MDCG 2021-24 11/11/2021
Live! #41 — Best Practices for Optimizing PMCF and Avoiding NB Findings 15/10/2021
Live! #40 — When should we throw the least burdensome flag or appeal an FDA decision? 01/10/2021
Live! #39 — Sustaining EU MDR and IVDR certification in the post-market phase - What will it take? 27/08/2021
Live! #38 — Best Practices in Site Transfer (or Consolidation) 23/07/2021
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