Scope

• Center selection, center feasibility assessment.

• Designing for Bioavailability - Bioequivalence Research.

• Designing together with researchers for phase research, observational and other clinical research.

• Ethics Committee & Ministry of Health application file and its annexes.

• Design of Research Protocol, Informed Voluntary Consent Form (BGOF) and Case Report Form (ORF).

• Monitoring activities (Monitoring)