Ad Hoc Clinical offers specific, ‘ad hoc’ research services and support.
We offer services as a functional ressource provider or as a partner CRO.
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…
Working with Ad Hoc Clinical means you enjoy all of the benefits of working with external staff but backed by the efficiency, expertise and availability of a professional organization.
Ad Hoc Clinical 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/ clinical investigations
As a privately owned company, the manager is committed to being personally involved and accessible.
Specific Areas of Activity
What do we do?
Site selections, site contract negotiations, Ethics and Competent Authority submissions, study start up activities, on site data abstraction, remote and on site monitoring, clinical project management, third party service provider selections, SOP writing, CRA training, consultancy.
For what type of studies?
Phase I to IV clinical trials, registries and non-interventional 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.
Key areas of focus
Auditing – Early Clinical Phases – Information – Late phase IV – People selection & placement – Project Management – Regulatory – Training & coaching