Bazelet is an EU-GMP certified developer of clinically-backed branded cannabis formulations and a CMO partner for white-label oils and flower. For over a decade we have studied the cannabis plant and its active compounds, and turned that work into a discipline: building medical cannabis products that perform like pharmaceuticals, with a defined composition that holds batch after batch.
The depth of that work is on record, and it extends well beyond Israel. More than 84 of our terpene-enriched oils, developed for different patient populations, are approved for marketing by the Israeli Ministry of Health. Our white-label oils have been approved for the German market, our branded products have passed regulatory approval in Australia, and we have exported medical cannabis flower to Germany at volume through our CMO. For a partner, that is evidence our products clear regulated markets, not a claim that they might.
Our formulations and production methods are protected by a portfolio of 60+ patent families, with granted patents across multiple territories. We are a formulation company, not a commodity supplier, and our clients range from medical cannabis companies to global pharmaceutical companies.
Our EU-GMP facility in Or Akiva is the largest cannabis production site in the Middle East. We run a strict quality program across the full chain, from the seed stage through research, development and finished product, with in-house laboratories that release every batch. Our EU-GMP facility in Malta supports reliable supply into Europe and other regulated markets.
For distributors, importers, pharmacies and pharma partners, the combination is what matters: a partner you can build a regulated-market business on, whether you carry our branded line or use us to manufacture your own.
Quality is controlled at every stage we touch, from the materials that enter our facility to the batch that leaves it. Our facility in Or Akiva holds IMC-GMP certification from the IMCA and EU-GMP certification from the Polish regulator. Our facility in Malta holds EU-GMP certification from the Maltese authorities.
Testing and stability are handled entirely in-house. Our own ISO 17025 accredited laboratories release every batch, and our stability chambers run the studies that establish shelf life and confirm products hold to specification over time.
Every input is gated before it enters production. Incoming flower and raw materials must meet regulatory requirements and pass our QA department before they are accepted. We work closely with our clients from start to finish, so the product they take to market meets their commercial goals.
Raw materials, intermediates and finished products are tested for pesticide residues, microbial contamination, molds, toxins and heavy metals, so that what leaves our facility meets a defined quality and safety standard, documented batch by batch.
For a partner, that is the part that travels: a full quality program and the documentation a regulated market expects, on every shipment.
Our formulations are developed, tested and released by the chemists, pharmacologists and QA specialists who run our laboratories day to day. That depth is what turns a defined specification into a product that holds batch after batch.
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