The most popular PMCF and PMPF questions from our clients
DEVICE L❤️VE Live! is a biweekly and interactive live show featuring expert panelists discussing timely topics, challenges, and solutions in the medical device industry. The panelists also answer audience questions. Every episode is added to our podcast, too.
Please view our blog for a other shows, as well as webinars, commentary from our experts, and more.
There's a lot of uncertainty in the industry around meeting the requirements of Post-Market Clinical Follow Up (PMCF) under the EU MDR and Post-Market Performance Follow Up (PMPF) under the IVDR.
Will what I have be enough or am I planning for too much?
How do I get the functions aligned... PMS, Regulatory, Risk, Clinical, Marketing?
It's not easy!
In this show we'll answer popular questions from our clients and as well as live audience questions. So please, bring your challenges to the table: we'll be ready!
Here's the panel:
Jon Gimbel, Ph.D. – Executive Director, Regulatory and Quality Consulting Services, and technical leader of R&Q CER/PER team
Ron Sills – Senior Principal Specialist (Former TUV Rheinland Lead Auditor through 2019)
Celeste Maksim, Ph.D. – Principal Consultant
Niki Caporali-Spaniel, RAC – Principal Specialist
Brian Hockett – Project Engineer