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Site Management Organization — India

Clinical Research.
Precisely Managed.

ClinTrust Research is a full-service SMO connecting global sponsors and CROs to investigator sites across India — with the precision, compliance, and speed modern trials demand.

8+
Specialized
SMO Services
ICH E6
GCP R3
Compliant
Pan-India
Site Network
Reach
24/7
Sponsor
Support
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ClinTrust Research is an SMO built from inside clinical research, not around it — a team with direct CRO and hospital research department experience, structured around getting site operations right from day one.

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What We Do

Everything your trial
needs to succeed.

From first submission to final archival — we manage every layer of site operations so sponsors can focus on science.

Site Identification & Feasibility Support
Assessing site readiness and protocol fit before commitments are made — feasibility evaluated against real capacity.
Investigator & Site Coordination
Direct, ongoing coordination with investigators and site staff to keep study execution aligned and on schedule.
Ethics Committee Documentation Support
EC/IEC submission documentation prepared and managed with the accuracy regulatory review demands.
Patient Recruitment & Retention Support
Structured support for identifying eligible patients and keeping them engaged through the full study duration.
Subject Visit Coordination & Follow-up
Visit scheduling and follow-up managed closely so protocol timelines are met without gaps in subject contact.
Source Document & Study File Management
Organized, audit-ready source documentation and study files maintained to inspection standard at every stage.
CRF/eCRF Completion Support
Case report form completion handled with the precision and consistency clean data collection requires.
GCP-Compliant Study Coordination
Every study coordinated under ICH GCP standards — compliance built into the process, not checked at the end.
CRO & Investigator Communication Management
Clear, consistent communication maintained between sponsors, CROs, and investigators throughout the study.
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Why ClinTrust

The SMO built for
serious sponsors.

We don't manage trials by volume. We manage them by attention — every site, every visit, every data point.

01
GCP-First Culture
ICH E6(R3) compliance isn't a checklist for us — it's the operating system. Every process, every person, every document.
02
Built-In Site Network
Pre-qualified investigator sites across India — faster activation, verified infrastructure, no guesswork on feasibility.
03
End-to-End Ownership
One team, one point of contact, full accountability from study start-up to close-out. No handoff gaps.
04
Trained CRC Workforce
Our coordinators come trained, not just recruited. GCP certified and protocol-ready before they set foot on-site.
05
Financial Transparency
Full payment visibility — sponsors and investigators both. No held funds, no ambiguity, full audit trail.
06
Sponsor-Aligned Speed
We understand sponsor timelines are non-negotiable. Our start-up processes are engineered for activation speed.
Compliance Standards
ICH GCP E6(R3) NDCT 2019 CDSCO Guidelines CTRI Registered Schedule Y ICMR Guidelines

Ready to discuss
your study?

Tell us about your protocol and we'll respond within 24 hours with a preliminary feasibility assessment.

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