SiteInsight Research connects global sponsors and CROs to India's most trusted clinical trial infrastructure — 120+ pre-qualified sites, 300+ GCP-certified investigators, AI feasibility in 24 hours.
SiteInsight Research is the dedicated Site Management Organisation of ProClin Research — one of India's most trusted CROs. We exist to solve the biggest cost-driver in global clinical trials: the time and effort to identify, activate and manage research sites in India.
Where a sponsor might spend weeks chasing individual hospitals and investigators, SiteInsight provides a single, accountable partner — with a pre-qualified, compliance-ready network already in place.
Talk to our team →Synopsis to shortlist, same day
Hospitals, polyclinics & NABL labs
GCP-certified, deployed & managed
Phase I–IV capability across all
Metro & Tier-2 India covered
Everything a sponsor needs to run a clinical trial in India — from site identification to study close-out — under one accountable roof.
120+ pre-qualified sites across metro and Tier-2 India. CDSCO-registered Ethics Committees at every site. Full compliance documentation maintained.
300+ GCP-certified PIs mapped by specialty, phase experience and enrolment track record. Interest confirmed before feasibility is submitted.
Protocol-briefed coordinators placed and managed by SiteInsight at each site. Source docs, EDC entry, visit scheduling — from day one.
Protocol synopsis to ranked site shortlist with patient pool estimates within 24 hours. India's fastest feasibility turnaround.
End-to-end EC dossier preparation, CDSCO coordination, regional-language ICF translations and audit-ready document management.
Community outreach, PHC referral networks and WhatsApp-based retention programs built for Indian patient populations.
AI-assisted ICF drafts, cover letters, SOPs and EC dossiers — reviewed by our regulatory team. Regional-language translations included.
Modular GCP certification for new PIs and CRCs. Protocol-specific training, audit-readiness workshops and inspection simulation.
A searchable registry of all 120+ qualified sites, filterable by therapeutic area, phase and region — with direct feasibility requests.
The full interactive site registry — with real-time search, TA filtering, PI profiles and AI feasibility — is currently in development. Full launch Q3 2026.
120+ sites qualified, documented and ready for listing
AI matching and ranking system — 75% complete
Full sponsor dashboard, shortlisting and request management
Get notified when the portal launches:
Every site, document and workflow governed by a quality framework spanning three jurisdictions.
Part 11-aligned e-signatures, immutable audit trails, role-based access controls.
Encrypted in transit and at rest. Least-privilege access with periodic review.
Version-controlled ICFs with regional translations and re-consent tracking.
Essential document management, inspection logs and CAPA at each site.
SiteInsight matches your specialty to sponsor pipelines and handles contracts, compliance and coordination.
Reviewed by our medical affairs team within 5 business days.
Our qualification team responds within 5 business days.
Send us a protocol synopsis — even a rough one. Our team returns a feasibility assessment, qualified site shortlist and enrolment projection within 24 hours, under full confidentiality.