The National Medicines Regulatory Authority (NMRA), an independent authority in the Ministry of Health established in 2015 through an Act of Parliament. NMRA plays a leading role in protecting and improving public health by ensuring medicinal products available in the country meet applicable standards of safety, quality and efficacy. The Authority regulates medicines, medical devices, borderline products, clinical trials and cosmetics. The National Medicines Quality Assurance Laboratory (NMQAL), charged with ensuring the quality of medicinal products, also functions under the purview of the NMRA.
Industry
Government Administration
HQ Location
120 Norris Canal Rd
Colombo 10, Western Province 01000, LK
Keywords
Assessing the need of a medicinal product to be made available to the publicRegistration and licensing of medicines that meet applicable quality and safety standards and are cost-effectiveProviding guidance on classification of medicinesmedical devicesborderline products and cosmeticsEnsuring medicinal products are appropriately manufacturedstoreddistributed and dispensedRegulating prices of medicinal products to ensure they are available to the general public at reasonable pricesRegistration and regulation of pharmacies to ensure they comply with good pharmacy practices