Commodity Guide · Air Freight

Pharmaceuticals

Cold chain, Health Canada DEL compliance, and DGR handling. ASEAN to Canada.

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DEL Required

Commercial drug imports

2–8°C

Standard cold chain

UN 1845

Dry ice classification

Free

MFN duty rate HS 30

Health Canada Requirement

A Drug Establishment Licence (DEL) is required for commercial pharmaceutical imports to Canada

A DEL is required for the Canadian importer of prescription/non-prescription drugs, APIs, and biologics. It is not required for Natural Health Products — those need a separate NHP Site Licence — or for genuine personal-use imports.

Source: Food and Drug Regulations (C.R.C., c. 870), Part C, Division 1A — Drug Establishment Licensing. Supporting guidance: GUI-0002 (Guidance on Drug Establishment Licences), GUI-0117 (Importing and Exporting Health Products for Commercial Use), GUI-0069 (Temperature Control of Drug Products during Storage and Transportation).

Relevant HS Codes

HS CodeDescriptionMFNCPTPPNote
3004.10Containing penicillins/derivatives with penicillanic acid structure, or streptomycinsFreeFree
3004.20Other, containing antibioticsFreeFree
3004.31Containing insulinFreeFree
3004.32Containing corticosteroid hormones, derivatives or structural analoguesFreeFree
3004.39Other, containing hormones or heading 29.37 productsFreeFree
3004.50Other, containing vitamins or heading 29.36 productsFreeFree
3004.60Containing antimalarial active principlesFreeFree
3004.90Other medicamentsFreeFree

Source: https://www.cbsa-asfc.gc.ca/trade-commerce/tariff-tarif/2026/html/00/ch30-eng.html

CPTPP savings on this lane

3006.70.90

Gel preparations - other (surgical/examination lubricant, coupling agent)

MFN 6.5%CPTPP Free

3006.93.10

Placebo/clinical trial kits - syrup based

MFN 6%CPTPP Free

3006.93.20

Placebo/clinical trial kits - sugar based

MFN 9.5%CPTPP Free

3006.93.30

Placebo/clinical trial kits - other food based

MFN 10.5%CPTPP Free

3006.93.40

Placebo/clinical trial kits - non-alcoholic beverages based

MFN 11%CPTPP Free

Canadian Import Process

Verify DEL

Confirm the Canadian importer holds a valid Drug Establishment Licence for the product category.

Cold chain booking

Book temperature-controlled handling with the carrier for biologics and vaccines.

DGR declaration

Declare dry ice (UN 1845, Class 9) on the AWB if the shipment uses cold chain packaging.

CBSA examination

Goods clear a CBSA examination against the commercial invoice and DEL reference.

Customs release

Shipment released to the DEL-holding importer for distribution.

Worked example

40kg of insulin, Mumbai to Toronto

A 40kg shipment of insulin (HS 3004.31) needs to move from BOM to YYZ. The fastest confirmed routing on that pair today is Emirates SkyCargo through DXB, at 1-2 business days.

Before booking, UAL verifies the Canadian importer's DEL covers insulin and biologics for that product category — insulin doesn't clear without it. Because insulin needs a 2–8°C cold chain for the full transit, temperature-controlled handling is booked directly with the carrier ahead of tender, not assumed available on the day.

If the packaging uses dry ice for the cold chain, UN 1845 (Class 9) is declared on the AWB with vented packaging confirmed before the shipment is accepted. On arrival at YYZ, CBSA examines the shipment against the commercial invoice and the DEL reference, then releases it to the DEL-holding importer for distribution.

Why ship pharma through UAL

DGR handling, taken seriously

UAL is IATA DGR certified. Every dry-ice and cold-chain declaration on this page is handled directly by our own trained personnel against the current IATA DGR edition, not routed to an outside partner.

Cold chain, booked directly

Temperature-controlled handling is booked directly with the operating carrier, not through a reseller layer that adds a markup and a communication gap between you and the aircraft.

Routing chosen on merit

We're not tied to one carrier's capacity or pricing. A pharma shipment routes via whichever carrier has the transit time, reliability, and cold-chain capability it needs that week.

DGR Warning — Class 9

Dry ice (UN 1845) requires prior carrier arrangement and vented packaging

Packaging must vent CO2. Prior arrangement with the carrier is required, and the AWB must carry the correct dangerous goods notation. Max 200kg dry ice per package on both passenger and cargo aircraft.

Read the full dry ice shipping guide →

Source: IATA Dangerous Goods Regulations, PI 954 — 200kg limit corroborated against the 67th Edition, effective 1 January 2026.

Frequently asked questions

A Drug Establishment Licence (DEL) applies to prescription and non-prescription drugs, active pharmaceutical ingredients, and biologics — this is the licence most commercial pharma importers need. Natural Health Products (vitamins, herbal supplements, homeopathic products) fall under a separate NHP Site Licence instead; a DEL doesn't cover them and an NHP licence doesn't cover drugs. If you're not sure which category your product falls into, that classification has to be settled before booking — it determines which licence CBSA will check for at clearance.

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Pharmaceuticals · 55 HS codes · CPTPP savings on 5 codes

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