Phase I–IV Clinical Trials
Support for interventional and observational studies across multiple therapeutic areas.
Capabilities
Clinical Research Capabilities
Phase I–IV trial support, biospecimen collection, diagnostic research, and bilingual participant recruitment — built for sponsors and CROs.
Biospecimen Collection Programs
High-volume collection with compliant chain-of-custody and processing workflows.
IVD and Diagnostic Validation
Clinical specimen acquisition and validation support for diagnostic assays.
Medical Devices
Clinical site support for device studies and technology validation programs.
Bilingual Participant Recruitment
Physician referrals, community outreach, digital and database recontact.
Feasibility Response within 48 Hours
Structured protocol review for sponsors and CROs within 48 hours.
Infrastructure
Site Infrastructure & Compliance
Purpose-built infrastructure for clinical trial execution, biospecimen collection, and diagnostic study support.
BSL-2 Laboratory
Certified Biosafety Level 2 facility for specimen processing and storage.
−80°C Ultra-Cold Storage
Long-term specimen preservation for demanding biospecimen protocols.
Cold-Chain Shipping
Validated dry ice, wet ice, and temperature-monitored courier shipping.
Barcode Chain-of-Custody
End-to-end traceability from collection through final delivery.
IRB & GCP Compliant
All protocols managed under active IRB oversight and GCP training.
HIPAA Compliant
Secure data management with full participant privacy protections.
Sponsors, CROs, & IVD Companies
Evaluate VRG for Your Next Study
Submit your protocol or study concept. Our team will assess feasibility, population fit, and operational readiness within 48 hours.