Merve CAN

Merve Can is a Regulatory Affairs Manager at Rigicon®, where they navigate FDA compliance and medical device regulations to ensure the company's products meet industry standards. With a solid academic background that includes Master's degrees in Pharmaceutical Biotechnology and Bioengineering from Marmara University, Merve has cultivated expertise in regulatory affairs and quality assurance. Previously, they served as a Medical Devices Lead Auditor at Notice, gaining valuable experience in ISO 13485 and the Medical Device Directive. Merve's professional journey also includes internships focused on vaccine production and research in bioengineering.