«BioEq» is experienced in conducting complex, intensive early and late stage clinical research and bioequivalence clinical trials.
- Experienced and dedicated staff
- Proven expertise in early phase
- Experience in phase II-III studies
- Big database of volunteers, patients
- Proven fast enrollment
- State-of-the-art facilities
- Quality management system
- Fast agreement signature process (not longer than 1-2 weeks)
- LEC review upon request
- LEC review before MoH approval which helps to speed up site start-up period of the trial
- Commitment to quality and the principles of Good Clinical Practice and applicable legislation
- Capacity to carry out multiple, complex, procedurally intensive studies simultaneously
- Customized solutions in the drug development process
We are interested in long-term relationship with our clients, that is why we try to make all possible efforts to perform clinical trials on time and with great quality.