Stop sourcing — start smart sourcing. GNH USA brings more than 15 years of experience in clinical-trial supplies, with direct relationships to innovators and manufacturers and a full audit trail from source to site.
Looking specifically for reference-listed drugs or active comparators? See comparator sourcing for clinical trials.
What we supply
Investigational and ancillary products
Clinical-trial supplies
Sourced IMP and ancillaries for sponsor-driven and CRO-managed trials.
IMP & comparators
Investigational medical products including biologics and biosimilars.
Rescue medication
Backup supply for emergent dosing scenarios.
Co-medication
Concomitant medicines required by protocol.
Analytical samples
Reference and analytical sample supply for laboratories.
Upstream reach
Sources from 60+ regulator-approved markets to supply trials worldwide.
Differentiators
What sets our clinical-trial supply apart
GDP-compliant warehousing
End-to-end Good Distribution Practice in our warehousing and supply chain.
Direct manufacturer relationships
Sourcing direct from innovators and OEMs — no intermediaries.
Audited supplier network
Locally audited and approved suppliers and manufacturers.
In-house personnel & facilities
Owned facilities monitored and supervised by an on-site Qualified Person.
Full audit trail
Source-to-site documentation for every shipment.
International standards
Compliance with ICH, FDA, EMA and WHO requirements.
Clinical-trial supply
Discuss your clinical-trial supply requirements
Share your organization, study-material requirements, quantities, delivery destinations and target dates. The team will assess the scope and clarify supply responsibilities.
FAQ
Frequently asked questions
What does GNH USA supply for clinical trials?
We supply investigational medicinal products (IMP), active comparators, rescue medication, co-medication and analytical or reference samples for both sponsor-driven and CRO-managed trials.
Which regulatory standards does your clinical-trial supply meet?
Our warehousing and supply chain operate under Good Distribution Practice (GDP), and we comply with ICH, FDA, EMA and WHO requirements.
Can you supply clinical-trial materials worldwide?
Yes. GNH USA sources from 60+ regulator-approved markets to supply clinical trials worldwide, with depot-to-site logistics and a full audit trail.
Do you provide a documented audit trail?
Yes. Every shipment carries source-to-site documentation, and our owned facilities are supervised by an on-site Qualified Person.
How quickly can you source clinical-trial materials?
Lead times depend on the product and market, but our direct manufacturer relationships allow fast sourcing. Send a Sponsor & CRO enquiry (gnh-usa.com/sponsor-cro-enquiry) for a specific timeline.
Related
Other services
Comparator Sourcing for Clinical Trials
Discuss comparator sourcing with GNH USA. Share the medicine, strength, quantity, source-market requirements and delivery timeline for your clinical trial.
Named-Patient Supply
Compliant supply of unlicensed and rare medicines for individual patients. WHO GDP-certified, with verified prescriptions and validated cold-chain shipping.
Validated Cold Chain Shipment
WHO GDP-validated cold-chain shipping for biologics, vaccines and temperature-sensitive medicines — qualified boxes and en-route temperature monitoring.