Consultancy & Management
Clinical Monitoring (CRA)
Monitoring visits by experienced, regulation-compliant CRAs
We conduct monitoring activities at investigative sites by assigning experienced clinical research associates (CRAs) who comply with applicable regulations.
Our CRA team handles the full spectrum across initiation, periodic and close-out visits — from source document verification to GCP compliance.
Scope
- Site initiation, periodic and close-out visits
- Source document verification (SDV)
- GCP compliance oversight
- Visit reporting and follow-up management
Related Services
Consultancy & Management
Research Consultancy
Feasibility, site recommendation and protocol consultancy
Consultancy & Management
CTR Management
Clinical trial agreements with public hospitals and foundations
Consultancy & Management
Payment Organization
End-to-end organization of site and volunteer payments