You have a need – before or after the CE marking – for a clinical investigation in accordance with DIN EN ISO 14155 to confirm the safety and performance of your medical device within the clinical evaluation?
Dr. Notghi Contract Research GmbH supports you in the implementation of the complex requirements of a clinical trial, and offers many years of experience in the planning and conduct of clinical trials.
We can assist you in the following study processes:
Our experts will gladly advice you personally. We look forward to your call or your message.