Medical Cannabis Cleanrooms
Angstrom Technology can support the medical cannabis industry by designing and building ISO and GMP cleanrooms. There are two areas where cleanrooms can support the production of cannabis-derived products.
- CBD extraction and oil production
- Medicinal cannabis cultivation, collection and processing into an Active Pharmaceutical Ingredient (API) or a Medicinal Product
Medicinal marijuana regulations
Medicinal marijuana products, like all medicinal products, must have either a Product License (Marketing Authorisation or MA), an Investigational Medicinal Product (IMP) licence for use in Clinical Trials or supplied as a Special under Regulation 167 of the Human Medicines Regulations 2012, and must be manufactured according to EU GMP guidelines.
Medicinal marijuana cultivation
For medicinal cannabis cultivation, a cleanroom envelope with the right HVAC system can create a controlled environment with the optimum growing conditions for producing the right cannabinoids. Cultivation areas, grow rooms, or hydroponic grow systems can be linked to GMP areas for processes such as drying, processing, packaging, and storing plant material.
MHRA-compliant cleanrooms
To comply with GMP guidelines, cleanrooms must control the level of airborne particulate and fulfil additional facility design requirements, e.g., fully-flush panels.
Medicinal products will need to be produced in a GMP cleanroom.
Cleanrooms for non-medicinal applications
ISO 14644-1 cleanrooms control airborne particulate levels and other environmental parameters—such as humidity and light—making them suitable for cultivation.
Non-medicinal products may be able to be produced in ISO cleanrooms.
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