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Saudi Arabia’s pharma drugs market worth $10bn, set to grow

This presentation comprised a briefing on the current situation of the practice of traditional medicine TRM and complementary and alternative medicine CAM , the availability of two kinds of herbal products, from local and imported crude medicinal plants, and the history of traditional medicine in Saudi Arabian culture. Yes, but the national authorities responsible for the regulation of herbal medicinal, traditional, complementary products and practices should authorize every advertisement before it reaches the public. The regulatory authority should issue an advertising permit after a satisfactory evaluation of the contents of the advert to ensure that the public gets the correct information about the product, devoid of ambiguous or false claims. The print and electronic media should be notified to ensure that every advertiser of herbal medicinal products obtains the advertising permit from the national authority before such advertisements are circulated. Medical claims: Medical claims are here defined as those claims specified to treat, cure or prevent a disease or restore, correct or modify physiological functions. Frequently, products with medical claims have to be registered by the medical products agency before being allowed onto the market. Nutrient content claims: Nutrient content claims, for instance, indicate that a certain product is particularly rich or low in a nutritional component such as fibre or fat. Pharmacies in Saudi Arabia are easily accessible to the public. Antibiotics, as well as many other non-prescription medications, are available OTC. This correlates with the findings of the present study, which indicated that the majority of respondents This is not surprising as many patients in Saudi Arabia can buy any OTC drug without any prescription. The current study revealed that the majority of patients use the OTC drugs without the advice of a health professional, as customers felt shy and reluctant, there was a lack of confidentiality, the pharmacist was felt to be impatient, there was a queue, or the customer did not trust the pharmacist. Meanwhile, a special label OTC for OTC drugs should be indicated in the advertisements for such non-prescription drugs. However, it is subject to the prior approval of the SFDA. The requirements for the importation of either traditional medicines or OTC products are generally the same as those for chemical drugs or prescription drugs. What are the regulatory requirements for traditional, herbal, complementary, or alternative medicines and devices? Can these traditional, herbal, complementary, or alternative products be advertised directly to the public? What health, advertising, and marketing claims may be made for traditional, herbal, complementary, or alternative products? What are the regulatory requirements for over-the-counter non-prescription medications? Are there any limitations on locations or channels through which OTC products may be sold? Please refer to Question 4 above. What health, advertising, and marketing claims may be made for OTC products? Can OTC products be marketed or advertised directly to the public? What is the mechanism by which a prescription-only product can be converted to an OTC product? What are the requirements for the importation of either traditional medicines or OTC products?

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