Xendo Drug Development B.V. expands its services with Clinical Research activities covering all aspects of your phase II – IV and medical device clinical studies.

Within the new business unit, the Study Management group ensures a timely handling of activities for clinical studies, such as submissions to the Ethics Committees (ECs) and/or competent authorities but also logistics of study materials. The Clinical Research Associates (CRAs) are experienced CRAs who conduct site management and monitoring. The monitoring services are conducted exactly according to the customer’s requirements. Xendo’s Data Management & Biometrics support the conduct of clinical trials from case report form design to the timely release of clean, high quality study data. Finally, the Medical Writing group is qualified to help you compile, organize, write, edit and produce a wide range of medical or scientific documentation required to support your product development efforts and regulatory submissions.

With the new business unit Clinical Research, Xendo ultimately aims at realizing the shortest through-put times of phase II – IV clinical studies.