- Guideline for safe disposal of expired & unwanted pharmaceuticals (Rev.No1)
- Guideline on recall of medicines, medical devices, & borderline products (Rev.No.1)
- Guideline on import control of pharmaceutical products & raw materials (Rev.No1)
- Guideline on procedure for expedited Marketing Authorization for Emergency use permission, registration/licensing of COVID 19 vaccines in Sri Lanka
- Guideline on Registration of Medicines
- Guidelines on Evaluation of Similar Bio therapeutic Products (SBPs)
- Biosimilars_EU-guide_2017
- Route of Administration
- Guidelines for Handling and Storage of Vaccines in the Private Sector
- Guideline on Advertising of Medicines & Medicinal Products to General Public
- Guideline on submitting registration sample to NMQAL
- Guideline on Labeling of Medicines
- Guideline on Variations for Medicines
- Guideline on Post Marketing Surveillance
- Guideline on Registration of Vaccines
- Guideline on Importing Medicines for Personal Use
Guidance documents
- Details