Elevate Your Clinical Evidence to Rank 4 in Hierarchy
Objectives
Gain an understanding of the clinical evaluation process in the post-market phase of the device
Learn how to define and plan appropriate strategies to meet requirements under the EU MDR
Hear our experts’ experiences to date from multiple manufacturers
Know more about the challenges other manufacturers may face and possible solutions
Get an insight into the tips, tricks, and pitfalls of PMS and PMCF under the EU MDR
Solve hypothetical case studies and benefit from an extended Q&A session
Reach Out To Us for the Full Webinar Recording
In case you missed the session, you can still access the full recording + 30-minute Q&A session with our experts.
Meet Our Speakers
Sumit Mehta
Founder & Chief Executive Officer
Prem Pandey
Head - EUMDR Compliance
NR Raghavan
Vice President – Global Operations
Speak with our PMCF team
Get a Rapid Assessment Of Your CER/PMCF Needs
Cetas Healthcare is a global leader in conducting ISO 14155-compliant Post-Market Clinical Follow-up (PMCF) surveys for MedTech devices. We specialize in designing and managing robust PMCF studies that capture real-world clinical evidence for Class II and III devices. To date, we’ve handled 25,000+ patient case forms, enabling clients to strengthen CE certification submissions and maintain full compliance with EU MDR requirements. By combining rigorous clinical research with actionable insights, we help MedTech companies continuously monitor device performance and enhance patient safety.
Contact Us: communication@cetas-healthcare.com
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