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The producers must be able to demonstrate safety and quality of the products before they are made commercially available, they must also hold evidence of their efficacy even though the regulatory body conducts some random and targetted reviews of small percentage of products each year. Listed products are considered low risk by the regulatory body (NAFDAC). However, where we lacks the appropriate technology for the analysis, it could be screen for safety/toxicity and listed for consumption, while the regulatory agency continue to keep surveillance on the listed herbs for any emerging adverse effect on the consumers. It became expedient to apply technology for appropriate elucidation/analysis of herbal medicines and its precursors before approval is being given. Moreover, since we cannot continue to assume that herbal medicine are devoid of adverse reactions and world Health Organisation has supported with evidence of documented recognisable adverse effects relating to consumption of some herbal medicines.

Another example- the Chinese herbal Medicine that are now registered. Herbal Medicines, being an integral part of healthcare system especially in Nigeria perhaps, because of our culture and belief, should be reinforced by ensuring that herbal Medicines are properly elucidated or analysed for registration as it is now obtainable in other climes such as India, where Ayuvedics are well promoted, they are now well packaged and registered. Please add comments at the bottom of the page Registration will allow the manufacturer to save and expand the process/business and create vast opportunity to generate post marketing data relative to that herbal medicinal product. Hence, NAFDAC should register instead of listing such products which implies that renewing would come every two years, imposing great financial burden for the manufacturer. While listing the herbal medicinal product is for two years, registration is for five years and applicants who have their products listed/registered are expected to submit a mandatory post marking surveillance report on the use, safety and adverse effects prfile of such products at stipulated intervals. To a large extent, the safety of herbal product is ascertained in Nigeria. Among other criteria, regulatory bodies such as NAFDAC in Nigeria would usually approve product for listing/registration on the receipt of a satisfactory laboratory reports of medicinal products/agents. In the Nigerian system, guidelines and criteria for registration and listing of herbal medicine and related products are essentially the same.

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