Clinical Trial

Clinical Research Unit Clinical Trial
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Accelerate Your Clinical Trial with a Trusted Academic Hospital Partner

Bring your study to life with the Clinical Research Unit (CRU) at RSUPN Dr. Cipto Mangunkusumo (RSCM). We support end-to-end clinical research execution — from feasibility and start-up to conduct, monitoring readiness, and close-out — powered by experienced investigators and hospital-wide clinical expertise.

Whether you are running an investigator-initiated study or a multi-center program, our team is built to deliver quality, speed, and regulatory confidence while keeping your study participant-first and data-driven.

GCP-Ready
Operations

GCP-Ready
Operations

Standardized processes, trained teams, and documentation discipline to protect quality and timelines.

Hospital-Wide
Clinical Depth

Hospital-Wide
Clinical Depth

Multi-specialty expertise from neonatal to geriatrics — enabling complex protocols and diverse populations.

Audit & Regulatory
Confidence

Audit & Regulatory
Confidence

Experienced in external audits and regulatory expectations — keeping your trial inspection-ready.

Real Capacity to Deliver — Not Just Promises

Our clinical trial ecosystem is backed by strong human resources, high patient volume, and cross-department collaboration — helping sponsors and investigators run studies efficiently.

  • 400+ GCP-certified investigators and research staff
  • 200+ total clinical trial projects supported
  • 50,000+ outpatient visits enabling recruitment potential

What you gain by running trials at RSCM:
access to diverse ethnicity and diagnoses, comprehensive hospital facilities, trained study teams, and a track record of meeting stringent audit and regulatory expectations.

Clinical Trial Ecosystem: Database, Trial, Facility

One Integrated Ecosystem: Facility, Database, and Study Execution

CRU is designed as a central hub where trial execution meets clinical reality. We connect the right clinic departments, research infrastructure, and operational workflows — so your study runs smoothly from first patient in to database lock.

1
Feasibility & Start-up Protocol review, resource planning, timelines, and startup coordination.
2
Study Conduct & Recruitment Support Site coordination, scheduling, and collaboration across specialties for patient access.
3
Quality, Documentation, and Audit Readiness Process discipline that helps maintain consistency, traceability, and inspection readiness.
Request Feasibility Discussion

Frequently Asked Questions

We support a wide range of clinical research, including interventional and observational studies, across multiple specialties. Share your protocol outline — we’ll advise on feasibility and site readiness.

Yes. Our team can support planning, stakeholder coordination, and operational workflows to reduce friction and improve timeline predictability.

RSCM serves a broad population with diverse diagnoses and clinical pathways, enabling access to varied study populations and specialty care networks.

Send your brief protocol synopsis and target timelines. We can schedule a feasibility discussion, align stakeholders, and map next steps for study initiation.