About our Site:

We have been conducting clinical trials since 1998. Our clinical study team includes specialists in:

  • internal medicine,
  • diabetology,
  • paediatrics,
  • dietetitians,
  • nurses,
  • midwives.

All our investigators and study site personel completed GCP courses and obtained valid certificates. Our team has got documented experience in conducting clinical trials. We use ERM, eCRF and IVRS systems. We have experience with both paper and electronic dairies.

Our center is located in the very center of the city with excellent access by public transport as well as by a car. Our site covers over XXXX square meter of space and has got multiple exam rooms. We have got separate room for monitoring visits and adequate space for storage of the drugs. Our center is equipped with three large waiting rooms, one on each floor to maximize patient satisfaction.


Equipment Onsite at Our Facilities Includes:

  • refrigerators,
  • freezers,
  • centrifuge,
  • weighing scales with height rods,
  • ECG Machines,
  • Ultrasounds,
  • secure storage,
  • on-site Emergency Equipment including AED,
  • Temperature Monitoring and Failure Alarm System of refrigerators and freezers,
  • Power Failure Alarm System,
  • computers.

Core clinical trias areas (trial indications):

  • Diabetes Type 1 And 2
  • Diabetes Mellitus
  • Dyslipidaemia
  • Oral and Technosphere Insulin
  • Hypertension
  • Neuropathy
  • Obesity


Contact detils:

Don’t hesitate to contact us with any questions you may have about our capabilities, facilities, or staff.
It’s difficult to list everything we have done, so if you don’t see something, please use the form below to contact us!

contact form


    • We use local IRBs. The EC gathers once a month, usually on the first Wednesday of each month.
    • Dedicated staff handle the initial regulatory packet to be submitted to the IRB.
    • Our PI is frequently appointed National Coordinating Investigator.
    • Initial Regulatory packets are submitted within two weeks of receipt.


    • We cooperate with sponsors on the basis of bilateral agreements. 
    • The contracts are signed by the owner of the site who is at the same time the Principal Investigator.
    • We usually respond to straightforward trial contracts within 3-5 business days.