The Astarta Clinical Research Center began active work in 2015. During this period, more than 50 clinical trials were launched in the following areas:
Astarta is a specialized center for clinical research. By specialized, we mean a highly qualified team, optimal organization of space and a professional approach to research and development.
Research success depends on the involvement of industry professionals. The main requirements for the staff of the center are English language proficiency, high computer literacy, openness and adherence to GCP standards. We managed to attract such employees to our team.
When designing the clinic, we were guided by the rule “Comfortable for the patient / convenient for the doctor”. During visits with a large number of procedures and / or intravenous infusions, the patient is provided with a day hospital ward. The researchers have at their disposal spacious rooms equipped with everything they need. We also did not forget to organize comfortable work places for the monitors during their visits.
The staff of the center understand that the main goal of their work is to obtain objective data on the investigational drug and to document it in a high quality manner. Primary documentation is maintained according to the ALCOA principles, the average speed of entering data into the KFM is 2 business days, responses to inquiries are 3 business days.
A professional team of coordinators providing support to physicians on technical and administrative issues throughout the study (work with CRF, investigator file, etc.).
At the time of checking the work of the center, employees of the sponsoring company are accommodated in comfortable rooms with wi-fi internet, computers and copiers. There is a comfortable dining area. The clinic is located 10 minutes walk from Primorskaya metro station, there are always free parking spaces.
Each study conducted has a separate, lockable material and drug storage area that is strictly restricted to study participants.
Researchers work in strict accordance with the principles of the GCP, the requirements of regulatory legal acts, as well as specially developed own SOPs.
Signing contracts with the institution and researcher within 5 working days. Consideration of the initial submission to the LEK within 14 days.
Researchers of our center are receiving appointments in the largest medical institutions of St. Petersburg and have an extensive referral network, which ensures active selection of patients in preparation for the launch of the study.