Cite Medical (CiteMed)

Cite Medical (CiteMed) specializes in regulatory services for medical device manufacturers, focusing on the European Union Medical Device Regulation (EU MDR) and In Vitro Diagnostic Regulation (IVDR). Their mission is to expedite the market entry of medical products while ensuring compliance with European Commission regulations. The company primarily offers Clinical Evaluation Reports (CERs), emphasizing systematic literature reviews that are essential for these reports. CiteMed utilizes proprietary software tools to enhance the literature search and review process, allowing for high-quality, timely outputs. They operate with a flexible model, managing the entire CER process or collaborating with clients' internal teams. Their services also include post-market surveillance activities, such as vigilance reports and Periodic Safety Update Reports (PSURs). CiteMed's global team consists of over 15 medical writers and regulatory experts, supported by project managers. They cater to a range of clients, from freelancers to large enterprises, and are known for their commitment to customer service, timely delivery, and maintaining compliance for their clients in the European market.

• Employees 6
• Founded 2017