AdHoc Clinical We are a small team of CRA’s, essentially offering study start up and monitoring services for  the pharmaceutical and medical device /IVD  industry.    We work in BELGIUM and FRANCE  and the Netherlands.   We offer specific, ‘ad hoc’ research services. More specifically, we are engaged in:  feasibility studies, site selection, site contract negotiations, translations, ethics submission, Clinical Trial Applications to the European MoH, on site data abstraction, on site monitoring, project management, interim management,…   Whether you require a single-service component or want to entrust us with a more complex project, we are ready to put our minds to work for you to deliver top quality data! We combine – high level international experience with local knowhow and expertise. This enables us to provide guidance and assistance at all stages of your clinical trials/ investigations..   As you would expect from a small team, we are flexible and reliable. Our commitment to a personal approach, direct communication and a quick response is highly valued by our clients. As a privately owned company, the manager is committed to being personally involved in overseeing the work being performed by the Ad Hoc team.  We are fluent in Dutch, French and English and have a basic knowledge of German and Spanish.