Food Supplement Registration in Sri Lanka - Overview
In Sri Lanka, food and dietary supplements fall under the “Borderline Category”, as they combine the characteristics of both foods and medicines. According to the National Medicines Regulatory Authority (NMRA) Act No. 05 of 2015, the NMRA is responsible for the regulation and control of food product registration in Sri Lanka, licencing, manufacture, import, and all other Regulatory aspects pertaining to borderline products.

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With growing population and increased focus on healthcare, the demand for Medical Devices is consistently growing in Sri Lanka. National Medicines Regulatory Authority (NMRA) is responsible for regulating Medical Devices in the country. It functions under the Sri Lankan Ministry of Health (MoH). Foreign companies must appoint a Sri Lanka Local Authorized Representative for assisting them with the Sri Lanka medical device registration process.


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Freyr is a global Regulatory leader providing services and solutions to Life Sciences companies in their entire Regulatory value chain. With our presence in 120+ countries, we help Life Sciences companies in their “local to global” journey. At Freyr Sri Lanka, we support companies to register their products with the NMRA, Regulatory strategy, market intelligence, in-country representation, PMS functions, and more. We also offer next-gen Regulatory software solutions covering the complete NMRA registration life cycle.


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