Good study monitoring is a major part and a key for sucessful studies. Therefore we personally guarantee that monitoring will only be done by qualified veterinarians experienced in conducting clinical trials

At site monitoring

Routine at-site monitoring consists of the check of all items stipulated in VICH-GCP such as
- CRF checks
- Data verification
- Adverse events
- Protocol and amendment compliance
- Drug accountability

In-house monitoring

Keeping contact to all study participants between the on-site visits is important to be up to date and as a general tool for controlling. In-house monitoring also consists of study file management, sponsor updates etc.