QMED CONSULTING

We provide strategic consulting services in connection with medical device approval as well as best-in-class expertise within clinical trial management (Qmed is a full service CRO), regulatory affairs, quality management and reimbursement and market access... Qmed provides services to ensure your compliance with critical regulatory markets, including EU and US regulations. With our extensive experience across all device classes, we are well-equipped to assist you in meeting regulatory requirements.

Also known as: Qmed

Primary location: Copenhagen K Denmark