dicentra is a full-service Contract Research Organization (CRO) and regulatory consulting firm specializing in safety, quality, and compliance for the global MedTech and life sciences industries. We offer tailored regulatory consulting and clinical trial services, supporting manufacturers of medical devices, advanced medical technologies, and life sciences products. Our expertise lies in helping your innovations gain access to both North American and European markets while ensuring compliance with all relevant regulations. With over two decades of experience and more than 24,000 successful projects, dicentra is your trusted partner in navigating complex regulatory landscapes and building confidence in your brand on a global scale.
