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ColdMatch facilitates sourcing and RFQs; it does not manufacture, sell, import or export the listed products and is not a regulatory authority. Suppliers are responsible for their products meeting the requirements of the origin and destination countries; buyers for import permissions, local rules and due diligence. Requirements vary by product and country, and the team checks requests before any supplier contact. Regulation and restricted items
Each package below adds specific requirements to a standard system type. Suppliers are asked to document how their offer meets each requirement, so offers can be compared on evidence rather than marketing.
These options usually cost more up front. Whether they pay back depends on your site, energy prices and operation — ColdMatch does not publish savings figures or price ranges.
Natural-refrigerant central plant specified with heat recovery, documented high-ambient design and remote monitoring.
Cold stores, distribution centres and processors planning a long-life natural-refrigerant plant.
Built-up cold store specified with documented panel performance, controlled door traffic and zone-level control.
Operators who need several temperature zones with tight control and full documentation.
Continuous monitoring with calibrated sensors, alarm escalation, audit trail and documents your quality team can qualify.
Medicine distributors, hospitals, laboratories and pharma cold-room operators.
Compressor rack and air coolers specified with efficiency features that suppliers must document, plus energy metering.
Buyers replacing or adding refrigeration who want efficiency features they can verify.
Links checked on . They explain rules and practice; they do not confirm that any specific offer complies. Requirements differ by country — check with your own advisers.
EU restrictions on certain fluorinated refrigerants by equipment type and date. Use it to check whether the refrigerant offered is restricted for your equipment in the EU.
US limits on higher-GWP HFC refrigerants in new refrigeration and air-conditioning equipment. Parts were under reconsideration in 2026, so check the current status before relying on a date.
US federal energy-conservation standards programme for commercial refrigeration equipment.
EU expectations for storing and distributing medicines, including temperature control, monitoring and qualification of premises and equipment.
Technical guidance on planning and carrying out temperature mapping of storage areas for time- and temperature-sensitive pharmaceutical products.
EU good manufacturing practice guidance; Annex 11 covers computerised systems such as electronic monitoring records.
US rules for electronic records and signatures used under FDA requirements.
Combine packages from this collection with individual systems in one shortlist, then send one request. Free for buyers; ColdMatch arranges projects from USD 250,000 and contacts suppliers on your behalf.
