Clinical Studies for Novel Pharmaceuticals and Biologics

ARS plans, organizes, monitors, and manages Phase I, II, III, and IV clinical trials in Russia. Among ARS Clients are Russian and foreign small, medium-size and big pharmaceutical and biotechnology companies. The range of services covers small local trials as well as complex international multicenter studies.

ARS takes an individual approach to its Clients and Partners.  The company can act either as a full-service CRO or a functional service provider.  Our areas of interest include projects with both local and international management.

ARS clinical research division is a team of certified doctors and pharmacists, worked for years for the leading multinational pharmaceutical companies and CROs. We operate in accordance with the ICH-GCP standards, international and local regulations and perform continuous internal quality control.

Our services include:

  • Clinical study planning
  • Project management
  • Clinical monitoring
  • Risk management
  • Sites’ selection and administration
  • Investigators’ training and support
  • Regulatory and ethics submission and approval
  • Sites’ contracting and payments
  • Quality assurance and control
  • Pharmacovigilance and medical monitoring
  • Logistics
  • Vendor management
  • Clinical study reporting

Clinical study basic feasibility is done for free. Please contact our Business Development team at to negotiate your potential clinical study’s details and obtain a project proposal.