| Guidelines on Submission of Documentation for Registration of Herbal Medicinal Products for Human use |
| GUIDELINES FOR IDENTIFICATION AND LABELLING OF PHARMACEUTICAL PRODUCTS |
| GUIDELINES FOR PRODUCT AND LOCATION MASTER DATA SHARING |
| Guidelines for registration of medical products for unmet medical needs |
| Guidelines for the Cancellation_Suspension of a registered medical product |
| Guidelines for variation of registered biological products |
| Guidelines on Reliance for Regulatory Decision-Making |
| Guidelines for registration of Human Biological Products |
| Guidelines for Variation to Registered Human Pharmaceutical Products |
| Guidelines for Registration of Pharmaceutical Products |
| Guidelines for Registration of Biosimilar Products |
| Guidelines on Abbreviated Procedures for Registration of Pharmaceutical Products-Version_3 |
| Guidelines for Renewal of Registered Human Pharmaceutical Products-Version_2 |
| Guidelines for Good review practices-Version 2 |
| Guidelines for Donation of Medical Products-Version_2 |
| Guidelines for Authorization for Emergency Use of Medical Products-Version_2 |
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