Pharmaceuticals & Biologics
Finished goods, intermediates, and high-value biologics — stored and distributed under cGMP and GDP in a facility purpose-built for temperature-sensitive product.
What we do for you
Audit-ready, in three temperature ranges
Pharmaceutical and biologics manufacturers arrive with a quality agreement, an audit schedule, and a list of things that must never happen. We store finished goods and intermediates across −35°C, +2°C to +8°C, and +20°C to +25°C, and we distribute direct to consignee.
Our quality management system, SOPs, validation records, and deviation and CAPA processes exist to support your regulatory obligations, not just ours — including when your customers or an authority come to look.
- Three qualified temperature ranges in one facility
- Allocated quarantine, hold, and release areas
- Validated equipment with scheduled requalification
- Deviation, CAPA, and change control processes
- Direct-to-consignee distribution
- Quality agreement executed alongside the MSA
More than plasma
Built for plasma, perfect for more
Fresh frozen plasma — source through finished goods — is what this company was built around, and the least forgiving product in the cold chain: no substitute exists for it, and it moves at −35°C. The validated ranges, quality system, and continuous monitoring that plasma demands are the same ones these products need.
GLP-1 and metabolic therapies
The rapidly expanding class of GLP-1 receptor agonists and other incretin-based, weight-management and metabolic injectables. These peptide therapeutics ship refrigerated at +2°C to +8°C and tolerate no gaps — we store and move them with continuous monitoring and excursion alarming, end to end.
Biologics and antibodies
Monoclonal antibodies, recombinant proteins, and other high-value biologic drug product and intermediates, stored and distributed within tight validated ranges from fill-finish to consignee.
Vaccines and sterile injectables
Refrigerated and frozen vaccines and other sterile injectables, handled under cGMP and GDP with allocated quarantine, hold, and release space.
Have an audit coming?
We'll host a facility walkthrough and share documentation ahead of it.