Merve Can Email and Phone Number

With a foundation in bioengineering and pharmaceutical biotechnology, my journey has been marked by a rigorous focus on regulatory affairs and quality assurance. At Rigicon®, my role as Regulatory Affairs Manager involves navigating the complexities of FDA compliance and medical device regulations, ensuring that our innovative urological solutions meet stringent industry standards.My previous tenure as a Medical Devices Lead Auditor at Notice fortified my expertise in ISO 13485 and the Medical Device Directive. These experiences have equipped me with a deep understanding of verification, validation, and quality management systems—skills that are essential in delivering excellence and fostering trust in the field of medical technology.