Cannabis Derived Medicine

The legal framework pertaining to cannabis-derived medicines in South Africa

Cannabidiol (CBD) containing medicines and processed products made from cannabis raw plant material, falling within the ambit of schedule 0 and meeting certain legal requirements, may currently be sold in open shops without registration.

We at Pharmalaw have been involved in the process which resulted in the exemption of these products from the operation of the Medicines Act. This initial exemption was followed by a rescheduling of these products in South Africa.

We have the necessary expertise to advise you regarding the legal framework pertaining to all aspects of cannabis containing medicines in South Africa.

The difference between licensing and registration pertaining to cannabis-containing medicines

Firstly, it is important to understand that registration refers to a medicine and licensing refers to a facility. Apart from cannabidiol (CBD) containing medicines and processed products made from cannabis raw plant material falling within the ambit of schedule 0, all cannabis derived medicines must be registered before sale, with exceptions. Facilities manufacturing, wholesaling, or distributing cannabis-derived medicines should be licensed.

FAQs

Do I need a license to sell CBD products in South Africa?
If you are a manufacturer, wholesaler, or distributor of cannabis derived medicines, including CBD containing medicines, you will require a license. At Pharmalaw we will provide you with the legal know-how to strategically plan your product journey.
Yes, but in adherence with strict provisions pertaining to the medicines as well as manufacturing, wholesale, and distribution facilities.