Sourcing
US-Licensed Supply Channels
FDA-approved products procured through a registered US wholesaler network.
Clinical Trial Supply
Dependable supply for US-linked clinical programs
For CROs, sponsors, and study teams, McHade provides comparator, RLD, biologic, and rescue sourcing through a registered US wholesaler — with the batch-level documentation trial QA teams expect.
Service lines
Three capabilities, scoped to your protocol
Each capability has distinct sourcing and documentation requirements for clinical programs. Explore the service that matches your study — then dive into the full service page.
Comparator & RLD Sourcing
Reliable procurement of US-licensed reference listed drugs and comparators with batch-specific documentation.
Comparator and reference listed drug (RLD) sourcing is often the first operational hurdle in a US-linked clinical program. McHade procures FDA-approved products through licensed US wholesaler channels, with batch-level documentation your QA and regulatory teams can file.
View service detailsSourcing Biologics & Biosimilars
Expert sourcing of complex therapeutics for clinical environments, including controlled-chain logistics.
Biologics and biosimilars introduce sourcing complexity beyond standard small-molecule comparators. McHade procures large-molecule therapeutics for clinical trial environments with cold-chain aware handling — 2–8°C where required — and the chain-of-custody documentation biologic programs demand.
View service detailsRescue Sourcing
Rapid sourcing support for trial disruptions, shortages, and unexpected protocol supply delays.
Trial supply disruptions — expired batches, supplier delays, unexpected protocol changes — can halt enrollment and jeopardize study timelines. McHade provides rescue sourcing support to recover supply through coordinated wholesaler network channels.
View service detailsOperational backbone
What supports every trial shipment
The sourcing and documentation infrastructure CROs and sponsors expect — when study timelines cannot slip.
Documentation
Batch-Level Traceability
Chain-of-custody and batch-specific records for trial QA teams.
Continuity
Rescue & Urgent Supply
Rapid sourcing when protocols fall behind schedule or stock runs short.
Compliance
Trial-Ready Paperwork
Documentation aligned to sponsor, CRO, and regulatory expectations.
Scope your clinical trial supply requirements
Share your protocol, comparator needs, product profile, and timeline. Our team will review the scope and respond with a compliant sourcing approach — turnaround depends on product complexity and regulatory requirements.