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Gene-Tech Consulting
a Technology-based business in information and life sciences for the biotech industry committed to sound corporate governance, integrity and efficiency.
REGISTRATION AND LICENSING REQUIREMENTS
*Licences to manufacture, import or export, or act as a wholesaler to wholesale and or distribute medicines are issued in accordance with the requirements of Section 22C read with Regulation 19 of the Medicines and Related Substances Act, 1965 (Act 101 of 1965)
*Licences for the manufacturer of Cannabis who is not exempted from the requirement to hold a licence and who wishes to cultivate, manufacture or import or who wishes to renew their existing licence to cultivate, manufacture or import.
*The licence to be subject to all the Standard Provisions applicable to Cultivator / Manufacturer's Licences under regulations for the time being in force under Section 22C of the Medicines and Related Substance Act, 1965.
**Complementary Medicines Manufacturing and Registration
*All medicines sold in South Africa must be registered by the Medicines Control
Council, [MCC], the Medicines Regulatory Authority set up under the Medicines and Related Substances Control Act [Act 101 of 1965] as amended, to control all aspects of the manufacture and sale of medicines.
* Fertilizers, Farm Feeds, Agricultural Remedies and Stock Remedies Act, 1947 (Act No. 36 of 1947).
*Veterinary Medicines.
We provide training and staffing to agencies that specialize in life sciences or bioinformatics, as well as management, sales and marketing services for science-based businesses, legal and paralegal services and bioengineering products, such as medical devices, robotic instruments and software.
"My vision is to legitimately research, produce, import, promote and distribute authentic, quality health orientated products which are both statistically and scientifically evaluated and qualified."
Gary Mark Jones
BSc(Pharm)UND(mps)
