Services > Clinical Research

Management and Monitoring of Phase I-IV Studies – Local and International
Preparing Full Set of Documentation for the Trial, Including Printing and Assembling
Bioavailability and Bioequivalence Methods and Studies
Selection of Centers and Investigators
Approval from Ethical Committees and Regulatory Authorities
Recruitment of Patients and Volunteers
Site Management Availability
Conducting of Investigator Meetings
Central Laboratories Establishment
Data Management and Statistics