«BioEq» is experienced in conducting complex, intensive early and late stage clinical research and bioequivalence clinical trials.

We offer:

  • 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.