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Covid 19 Vaccines Procedures and Reports

Guideline on procedure for expedited Marketing Authorization for Emergency use permission, Registration/Licensing of COVID 19 vaccines in Sri Lanka

The National Medicines Regulatory Authority accepts applications of vaccines against COVID 19 to be considered for emergency use authorization / registration. COVID 19 vaccines are eligible for rapid regulatory review under section 109 of the NMRA Act No. 5 of 2015 and related guidelines. 

Expression of Interest (EOI) to National Medicines Regulatory Authority by Applicant of COVID-19 vaccines

Application format for Expedited Marketing Authorisation



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