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national medicines regulatory authority (nmra) - sri lanka home about us overview organization structure acheivements activities planned activities messages drugs drugs registration new chemical entities (nce) quality failures devices regulatory information quality failures cosmetics regulatory information clinical trials regulatory information clinical trials subcommittee local manufacturers drugs news tenders contact us skip to content  vision achieve a healthier nation by ensuring the provision of safe, quality and efficacious medicinal and cosmetic products (therapeutic goods). read more mission to regulate and control the manufacture, importation, sale, storage and distribution of cosmetics, devices and drugs (including nutraceuticals and ... read more drugs quality drugs for better life read more welcome to national medicines regulatory authority (nmra) - sri lanka the national medicines regulatory authority (nmra) is the institution in which the ministry of health has vested the authority to ensure that the pharmaceuticals and medical devices available to the public meet the required standards of quality and are within the existing legislative framework with respect to the production, marketing and dispensing of these items. latest news patient information leaflets in local languages reminder to all pharmaceutical manufacturers and importers nmra wishes to remind you that the decision to include a patient information leaflet in sinhala and tamil languages on the following prescription on patient information leaflets in local languages reminder to all pharmaceutical manufacturers and importers nmra wishes to remind you that the decision to include a patient information leaflet in sin... read more wholesale and retail prices of biological products notice to all local agents of medicines. please submit the wholesale and retail prices pertaining to all biological products including vaccines which are being imported by your company on or bef... read more registration on priority basis. registration on priority basis notice since the number of registered suppliers are limited, nmra has decided to entertain new applications for following products and priority evaluation will be ... read more further to notice published on 30.05.2017 notice further to notice published on 30.05.2017 to all representatives of importers with effect from 15th august 2017, those who submit applications for registration of medicinal produc... read more dollar rate for revised fees notice dollar rate for revised fees 1. revised fees will be charged in sri lankan rupees. 2. the selling rate (usd : slr) published by the central bank for the last day of the preceding mon... read more adverse drug reactions advertisements good manufacturing practices product recalls application forms legislation guidelines publications who collaborated activities complaints alternative therapeutic products important links home --   -- skip to content copyright © 2018 national medicines regulatory authority (nmra) - sri lanka. all rights reserved. powered by pooranee inspirations. last update: 23-05-2018. sitemap | disclaimer

URL analysis for cdda.gov.lk

http://nmra.gov.lk/index.php?option=com_content&view=article&id=310%3apatient-information-leaflets-in-local-languages-reminder-to-all-pharmaceutical-manufacturers-and-importers-nmra-wishes-to-remind-you-that-the-decision-to-include-a-patient-information-leaflet-in-sinhala-and-tamil-languages-on-the-following-prescription-on&catid=3%3alatest-news&itemid=123&lang=en'
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