Based on international experience from many years of working with clinical research as well as marketing activities in the medical industry, the Consultancy Trial-Support is able to carry out a wide range of tasks related to clinical reseach and development of health care technology. 
 During decades of working with clinical trials, an extensive network has been built up within clinical research units in the health sector, in the medical industry and in Contract Research Organisations (CRO).
 To be able to offer Comprehensive full-service support for major projects, we do collaborate with national and institutions and with Contract Research Organisations to ensure sufficient capacity and the best knowledge and experise tailored for the specific purpose. 
Gastroenterology and Oncology are our main experiences but other areas of pharmacology and therapeutics are also covered by Trial-Support.
The objective for the Consultency Trial-Support is to be a qualified support for the promotion of clinical research and for the best diffusion of scientific knowledge gained.

We offer:
- Conduct of clinical trials, local as well as international
- Handling of Regulatory Affairs such as applications for Authorities
- Monitoring of clinical trial of all phases according to the Guidelines for Good Clinical Practice
- Arrangement of different kind of meetings in relation to the trials
- Educational activities including team development of the staff at clinical research units
- Preparing and writing of study documents and forms and description of procedures
- Medical writing of clinical reports, posters and other kind of presentations
- Facilitation of co-operation between clinical research units and the industry

Trial-Support

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