- 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 for safe Disposal of Expired & Unwanted pharmaceuticals
- Guideline on Import control
- 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
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- விவரங்கள்