Pharmaceutical Cold Chain — Storage & Transport
One partner for the full pharmaceutical cold chain. ColdMatch sources GDP-qualified storage (+2/+8°C, -20°C, -80°C, cryogenic) and validated transport (active containers, PCM shippers, GDP reefer) from vetted manufacturers, EPC contractors and logistics providers worldwide — with project financing available.
Why source with ColdMatch
+2/+8°C GDP storage
Qualified pharma cold rooms with mapping, monitoring, backup power and redundancy per EU GDP and WHO TRS.
-20°C & -80°C freezers
Frozen and ultra-low freezers for vaccines, biologics, mRNA products and long-term biobanking.
Cryogenic & LN₂
Cryogenic vaults, dewars and vapor shippers for cell & gene therapy, stem cells and reproductive medicine.
Active air containers
RKN, RAP, CSafe RKN/VVL and Envirotainer active containers for global GDP air freight.
PCM & dry-ice shippers
Passive PCM parcels and dry-ice shippers with validated performance envelopes and data loggers.
IQ / OQ / PQ documentation
Full qualification packs, temperature mapping studies and validation protocols with every project.
GDP / GMP compliance
Suppliers audited against EU GDP, WHO TRS 961/992, USP <1079> and local pharma authorities.
Turnkey pharma warehouses
End-to-end GDP cold storage warehouses with EPC delivery, controls, BMS and financing.
Global reach
Sourcing across EU, US, MENA, LATAM, Africa and Asia — with import finance and logistics arranged.
Typical specifications we source
- CRT storage
- +15 to +25°C
- Refrigerated storage
- +2 to +8°C
- Frozen storage
- -20°C
- Ultra-low storage
- -80°C (ULT)
- Cryogenic storage
- ≤ -150°C (LN₂)
- Active air containers
- RKN / RAP / CSafe / Envirotainer
- Passive shippers
- PCM parcels, dry-ice, VIP
- Data loggers
- Single-use & reusable, real-time
- Compliance
- EU GDP · WHO TRS · USP <1079> · GMP
Frequently asked
What temperature ranges do you cover for pharmaceuticals?+
Controlled Room Temperature (+15/+25°C), refrigerated (+2/+8°C), frozen (-20°C), ultra-low (-80°C) and cryogenic (LN₂, -150°C and below) — sourced from GDP/GMP-qualified manufacturers.
Is your cold chain GDP compliant?+
Yes. Every sourcing partner delivers IQ/OQ/PQ documentation, temperature mapping and qualification protocols aligned with EU GDP, WHO TRS 961/992, USP <1079> and local pharma authority requirements.
Can you handle both storage AND transport?+
Yes. ColdMatch sources both sides of the pharma cold chain: qualified cold rooms, ULT freezers and cryogenic vaults on the storage side; active pharma containers (RKN, RAP, CSafe, Envirotainer), passive PCM shippers, dry-ice solutions and validated GDP road/air freight on the transport side.
What about clinical trials and biotech samples?+
We source ULT freezers, LN₂ dewars, sample transport in dry shippers and specimen logistics for CROs, biotech and cell/gene therapy programs — including cryogenic vapor shippers for autologous therapies.
Do you cover last-mile pharmacy and hospital delivery?+
Yes. Validated last-mile solutions with data loggers, real-time monitoring and chain-of-custody documentation from central warehouse to pharmacy, hospital or clinic.
Can I finance pharma cold chain infrastructure?+
Yes. ColdMatch connects qualifying projects with lenders offering equipment finance, project finance and import finance for GDP cold storage and validated transport fleets worldwide.
How fast do I get supplier proposals?+
Most pharma buyers receive shortlisted proposals from qualified GDP/GMP suppliers within one business week of submitting a request — free for buyers.
Get matched with vetted suppliers in 48 hours
One RFQ — multiple competitive quotes from manufacturers, EPC contractors and turnkey providers worldwide.
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