Ad Hoc Clinical offers specific, ‘ad hoc’ research services and support . More specifically, we are engaged in feasibility studies, site selection, site contract negotiations, translations, Ethics submission, CTA submissions, on site data abstraction, remote or/and on site monitoring, project management, consultancy…
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.
Working with us means you enjoy all of the benefits of using individuals as external staff but backed by the efficiency, expertise and availability of a professional organization.
Adhoc combines high level international experience with local knowhow and expertise. This enables us to provide guidance and assistance at all stages of your clinical trials.
We operate in Belgium, The Netherlands and France.
As a privately owned company, the manager is committed to being personally involved in overseeing the work being performed by the Ad Hoc team.
Specific areas of activity
What do we do?
Site selections, site contract negociations, Ethics and Competent Authority submissions, study start up activities, on site data abstraction, remote and on site monitoring, clinical project managament, third party service provider selections, SOP writing, CRA training, consultancy.
For what type of studies?
Phase I to IV clinical trials, registries and non-internvetional studies, Pass Studies, Academic research, Clinical Investigations pre and post CE label, Performance Evaluations studies for IVD's
Who are our clients?
Large CRO's, Biotech industry, Medical Device Industry, IVD industry, universities.
Auditing Late phase IV People selection & placement Training & coaching Regulatory Other Information