One building, designed and constructed to EU-GMP standards.
Purpose-built around pharmaceutical quality systems and GMP principles, for third-party contract manufacturing and packaging.
- Built to EU-GMP standards
- Classified, pressure-cascaded
- Schedule 6 vault, restricted access

What is GMP?
Good Manufacturing Practice is the set of rules a regulator holds a pharmaceutical manufacturer to. It governs the building, the equipment, the people and, above all, the paperwork that proves what happened to a batch.
A legal standard, not a marketing one
Good Manufacturing Practice is what a medicines regulator requires of anyone making a pharmaceutical product. It is inspected, and it is granted or withheld.
The building is part of the product
Classified cleanrooms, controlled air pressure between rooms, filtered air, and product and personnel kept on routes that never cross.
Everything is written down
Documented procedures, batch records, deviation and CAPA management. If it is not recorded, an auditor treats it as not having happened.
Release is a decision somebody signs
Material is quarantined by default. It leaves only when quality control and the Responsible Pharmacist have signed for it.
Become a supplier.
We buy medical-grade flower from GACP-registered cultivators across South Africa. If you are licensed and growing, tell us what you have and we will take you through qualification, audit and approval.
Come and walk the floor.
We are set up to host customer due-diligence visits and on-site audits, and we would rather show you the building than describe it. Contact us to arrange a walkthrough.






