Clinical Services
Advantages of Performing Clinical Trials in Colombia
- Timelines for regulatory approvals (IRB/MOH) are short - the average is 17-20 weeks.
- Sites located in different cities other than Bogota (i.e. Medellin, Cali, Bucaramanga, Pereira, Barranquilla, ) with good accessibility for monitoring and study activities (i.e., air transportation).
- A good number of patients in different indications.
- There are a good number of investigators, hospitals and clinics with experience in clinical trials, including private consulting rooms allowed to conduct clinical trials of different phases.