MatrixPharm offers a full range of top-quality clinical research services (Phases I – IV) in Russia and the CIS countries, serving the pharmaceutical industry worldwide.
Our trained specialists are experienced in carrying out clinical trials in numerous fields of medicine. They regularly take part in certified ICH-GCP training programmes, as well as training in monitoring and in clinical trial project management.
MatrixPharm offers its Clients maximum flexibility. We provide each one of the following services on a stand-alone basis, or in any combination that meets your needs:
- Monitoring and Co-monitoring (Phases I – IV)
- Project Management
- Study Protocol Development
- CRF Designing
- Study Design Consultation
- Preparation of Information for Patients
- Preparation of Informed Consent forms
- Study Feasibility
- Selection of Study Centres
- Site Management
- CTM Management
- Regulatory Issues
- Submission of applications to central and local ethics committees
- Bioequivalence and Bioavailability Studies
- Financial Management of the Clinical Trial
- Management of investigators' fees
- Arrangement of the investigators' start-up and follow-up meetings
- Study Initiation and Closeout Visits
- Translation of documentation related to the clinical trial, from English into Russian and vice versa
