Clinical Research Trial Workflow
Feasibility
Our site evaluates the practicality and scientific validity of a proposed research study before initiation.
Site Selection Visit
The sponsor/CRO visits our facility to assess infrastructure, compliance, and site readiness for the study.
IRB Submission
The Institutional Review Board ensures that study protocols protect human rights and meet ethical standards.
NBC Submission
The National Bioethics Committee conducts a detailed ethical review to ensure compliance with national standards.
Trial Agreement & Budget
A formal contract defines responsibilities, payments, and regulatory requirements between SCRC and the sponsor/CRO.
DRAP Submission
The protocol is submitted to DRAP to confirm the safety, efficacy, and quality of the therapeutic goods involved.
Site Activation
Following DRAP approval, the site is officially activated, and trial operations commence under regulatory supervision.
DSMB Oversight
The Data Safety Monitoring Board continuously tracks study progress to ensure participant safety and compliance.
Collaborators
