Dr. Hatem Rabeh, Author at Medical Device Navigator

Author name: Dr. Hatem Rabeh

Dr. Hatem Rabeh, MD, MSc Ing, is a clinical evaluation expert and the founder of Medical Device Navigator. With a background in medicine (MD) and medical engineering (MSc, Université Grenoble Alpes), he specializes in EU MDR clinical evaluations, PMCF strategies, and FDA regulatory pathways. He has published peer-reviewed research in interventional radiology and medical device innovation, and is a recognized speaker at international medtech conferences. Dr. Rabeh founded Medical Device Navigator to democratize access to medical device regulatory information worldwide.

Webinars

BSI Webinar: MDR General Safety and Performance Requirements – Practical Guidance

Dr. Hatem Rabeh /

BSI notified body webinar covering the general safety and performance requirements (GSPR) under the EU Medical Device Regulation, with practical […]

Webinars

TÜV SÜD Webinar: Clinical Evaluation of Medical Devices Under EU MDR

Dr. Hatem Rabeh /

TÜV SÜD training webinar on clinical evaluation requirements for medical devices under the EU MDR, covering clinical evaluation plans, literature

Webinars

Mantra Systems Webinar: Post-Market Surveillance – PMCF and Vigilance Under EU MDR

Dr. Hatem Rabeh /

Webinar on post-market surveillance requirements under the EU MDR, focusing on Post-Market Clinical Follow-up (PMCF) studies, vigilance reporting, and periodic

Webinars

QbD Group Webinar: EU MDR Bottleneck 2026 – Strategies for Medical Device Manufacturers

Dr. Hatem Rabeh /

With notified body capacity constraints creating bottlenecks in 2026, QbD Group experts discuss strategies for medical device manufacturers to navigate