20 May - 21 May
Sponsored By:
RQM+ is committed to maintaining our unrivaled collective knowledge through internal learning initiatives, but we don’t stop there. We share our expertise with other regulatory and quality professionals to lift up the entire industry. Visit this page often to see what’s new.
Mon-Tue
20-21
Wed
22
22 May
2:30 PM - 3:30 PM ET | 8:30 PM - 9:30 PM CET
Sponsored By:
Virtual Event
Speakers:
David Novotny, Chief Operating Officer, Trial Services - RQM+
John Reites, CEO - THREAD
See MedTech study examples that utilize hybrid study approaches to accelerate patient recruitment.
Register NowThu
23
23 May
9:00 AM - 9:45 AM ET | 3:00 PM - 3:45 PM CET
Sponsored By:
Virtual Event
Speakers:
Ed Ball, CEng, MIPEM, MIMMM - Manager, Intelligence & Strategic Execution
Join us for an eye-opening 30-minute presentation and additional 15 minutes of Q&A, where RQM+ Manager of Intelligence and Strategic Execution, Ed Ball, MSc CEng MIPEM, will explore the vital role of communication throughout the risk management activities conducted over the course of the medical devices lifecycle. Drawing from his extensive experience in the industry, having worked for the UK’s MHRA and several device manufacturers, Ed will share insights and strategies to help you elevate your risk management processes.
Register NowThu
06
06 June
11:00 AM - 12:00 PM ET | 5:00 PM - 6:00 PM CET
Sponsored By:
Virtual Event
Speakers:
Mark DuVal – President & CEO, DuVal & Associates, P.A.
Allison Komiyama, Ph.D., RAC – Vice President, MedTech Innovations, RQM+
Jon Gimbel, Ph.D. – Vice President of Technical, RQM+
Erin Gontang – Senior Consultant, RQM+
Jaishankar (Jai) Kutty, Ph.D. – Vice President, Global Regulatory Affairs (moderator)
The FDA's recently proposed rule on wound care products has sent ripples through MedTech. This rule, if finalized, could significantly impact the classification, labeling, and testing requirements for a wide range of wound care devices. This online panel is your key to understanding the potential implications of this rule on your products and to prepare for the changes. In this conversation, our team of FDA regulatory experts will examine the proposed rule, providing valuable insights and actionable strategies to help you navigate what's next for wound care devices.
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