How is UK medical cannabis tested, irradiated and released?
This is the part of the system that most clearly separates a prescribed medicine from anything bought illicitly, and it is also the part patients hear least about. It is worth knowing what has happened to a product before it reaches you.
The short answer
- Every batch is tested before release, and the results are recorded on a certificate of analysis.
- Testing covers more than cannabinoid content — microbial contamination, pesticides and heavy metals are all in scope.
- Some flower is irradiated to reduce microbial contamination, which is a safety measure rather than a shortcut.
- Batches carry a number, so a specific container can be traced back to its test results.
- Import is licensed per consignment, which is one reason a preparation can become unavailable.
Why any of this is necessary
Because plant material is a biological product, and biological products carry risks that a purified molecule does not: mould and bacteria from growing and drying, residues from cultivation, and variation between harvests.
The people receiving these medicines include patients whose immune systems are suppressed by other treatment, for whom inhaling fungal spores is a serious risk rather than a theoretical one. That single fact drives most of the processing described below.
It is also the substantive difference between prescribed and illicit supply, which is set out in How is medical cannabis different from street cannabis?
What a certificate of analysis covers
A certificate of analysis is the laboratory record for one specific batch. It states what was tested, by what method, and what was found.
- Cannabinoid content, so the preparation matches its specification
- Microbial testing, including yeasts, moulds and specified bacteria
- Pesticide residues
- Heavy metals, which plants can take up from growing medium
- Residual solvents, where an extraction process has been used
- Moisture and, for some products, foreign matter
Your pharmacy holds this information, and a batch number on the container links what you have to the specific record. There are glossary entries for certificate of analysis and batch number.
Why some flower is irradiated
Irradiation is used to reduce microbial contamination to a level acceptable for a medicine. It does not make the product radioactive, and it is used across food and pharmaceutical manufacturing for the same reason.
Dried plant material cannot be heat-sterilised without destroying it, so where microbial levels exceed the standard, irradiation is one of the few options. Both electron beam and gamma methods are used.
Patients do raise a fair objection: there is evidence that irradiation can reduce terpene content, and some people report a difference in smell and taste. Whether that translates into a difference in effect is not well established, and the trade-off is being made against a documented contamination risk rather than a theoretical one.
Not every product is irradiated. If it matters to you, it is a reasonable thing to ask your clinic or pharmacy about a specific preparation, and there is a glossary entry for irradiation.
Batch release, import and why supply changes
Before a batch can be supplied in the UK it has to be released, which is a formal check that it was made to the required standard and meets its specification. Unlicensed products are also imported under licence.
That combination — per-batch release plus per-consignment import licensing, on top of a Home Office controlled drug licence — is why supply of a particular preparation is less predictable than for an ordinary licensed medicine. A delay anywhere in that chain shows up as a product being unavailable.
It is the most common practical frustration patients report, and it is a structural feature of the specials route rather than a failing of any one clinic. The background is in Why is medical cannabis an unlicensed medicine in the UK?
Flower, granulate and extracts
The same quality requirements apply whatever the form, but the processing differs. Granulated preparations are milled plant material, which changes handling and dosing consistency rather than the underlying medicine.
There are glossary entries for flos, granulate and full spectrum. How each is used is covered in How are cannabis-based medicines taken?
Frequently asked questions
What is a certificate of analysis?
The laboratory record for one specific batch, stating what was tested and what was found — cannabinoid content, microbial contamination, pesticides, heavy metals and, where relevant, residual solvents. The batch number on your container links to it.
Why is medical cannabis irradiated?
To reduce microbial contamination to a level acceptable for a medicine. Dried plant material cannot be heat-sterilised without destroying it, and some patients receiving these medicines are immunosuppressed, for whom inhaling fungal spores is a serious risk.
Does irradiation damage the product?
There is evidence that it can reduce terpene content, and some patients report a difference in smell and taste. Whether that changes the clinical effect is not well established. Not every product is irradiated, and it is reasonable to ask about a specific preparation.
Why did my preparation go out of stock?
Unlicensed products are released batch by batch and imported under licence per consignment, on top of controlled drug licensing. A delay anywhere in that chain shows up as unavailability. It is a structural feature of the specials route.
Sources and further reading
Every factual statement on this page is drawn from the following public sources. Links open in a new tab and are not affiliated with Flora House.
- MHRA: The supply, manufacture, importation and distribution of unlicensed cannabis-based products for medicinal use
- MHRA Guidance Note 14: The supply of unlicensed medicinal products (PDF)
- GOV.UK: Cannabis, CBD and other cannabinoids — drug licensing factsheet
- NICE guideline NG144: Cannabis-based medicinal products
- NHS: Medical cannabis (and cannabis oils)