Clinical trials in drug development are a vital part of the process to bring new medicines to patients. We have recognized this need and offer flexible and fast services that can be custom tailored, specifically to meet all study protocols. We have specialists with knowledge of all study phases and can deliver an optimized configuration of operations such as:
- Administrative tasks
- Data processing (eCRF)
- Quality control
- Training study nurse
- (Pre-)screening calls
- Preparing (home) visits
- Conducting (home) visits
- Blood sampling
- Sample processing
- Transport of samples
- ….
We can temporally take over internal roles to allow your permanent staff to focus on patient related activities. Our clinical site support services help to stay cost effective while meeting your study objectives in a swift manner.
Let’s talk! Contact us to learn what we can do for you.