National Medicines Regulatory Authority (NMRA) Sri Lanka

About

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.

Keywords

recommending appropriate amendments to relevant laws pertaining to regulation of medicinal products, borderline products & cosmetics, distributed & dispensed, regulating prices of medicinal products to ensure they are available to the general public at reasona, ensuring promotion & adverting is fair, regulating all matters pertaining to the conduct of clinical trials, registration & regulation of pharmacies to ensure they comply with good pharmacy practices, supporting postmarketing surveillance, ensuring medicinal products are appropriately manufactured, stored, educating the general public on proper use of medicinal products, medical devices, registration & licensing of medicines that meet applicable quality & safety standards & are cos, supporting initiatives for local manufacture of medicinal products, providing guidance on classification of medicines, balanced & evidencebased, assessing the need of a medicinal product to be made available to the public

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