Dania Qreyeah is a Regulatory Affairs and Business Consultant specialising in medical devices and pharmaceuticals. She focuses on EU MDR, ISO 13485, and global regulatory frameworks, with a proven track record supporting companies across Europe and the MENA region.
She has successfully led EU MDR certification projects for non-EU manufacturers, authored Clinical Evaluation Reports approved by Notified Bodies, and served as PRRC, ensuring compliance with post-market surveillance, vigilance, and quality system requirements.
Dania bridges technical, regulatory, and strategic functions, making her a trusted partner for companies navigating complex regulatory pathways in both the EU and MENA markets.