Finding and selection of clinical study sites/centres
- Preparation of feasibility studies.
- Authorisation of clinical studies (National Institute of Pharmacy – Medical Research Council), informing local ethics committees.
- Selection of investigators, organisation of trainings.
- General contacts with study sites and with the Sponsor.
- Starting clinical studies.
- Full monitoring processes (source, drug, CRF, investigator and patient folders).
- Management of study sites towards vendors, the Sponsor and local ethics committee.
- Closing clinical studies and sites.
- Organising, performing, and monitoring clinical trials/studies of medical and diagnostic devices.
- Organising, performing, and monitoring trials/studies of veterinary medicinal products and/or devices.
TCRA / CTA work offering
- Training/provision of, and, at the request of our Clients, finding Clinical Research Associates (CRA/monitor).
- Training/provision of, and, at the request of our Clients, finding Clinical Trial Assistant (CTA).
Why use 3rd party CRA?
Flexible contracting in short time
You have access to highly qualified staff immediately
The study will get in experienced hands at any stage
Thus the handing over of an ongoing study is performed in the shortest possible time
Saving staff costs (health and pension insurance contributions, sickness benefit, business car, cell phone, laptop)
Further savings in the case of home-based work (operational office costs, rent, heating, lighting, office furniture, cleaning, office equipment, telephone costs, operation of computers, printers, photocopiers, scanners, faxes)
More..
Develop medical devices providing service from authorisation, through organization to implementation.
Develop drugs and medical devices for veterinary medicine. Full service from site selection, through authorisation, organization to implementation.
