1. National Drug Policy 2007
2. Guideline for Regulating Health Supplements
3. Guideline for Registration of Transfusion Transmissible Infections(TTI) test kits
4. Interim Guidelines for regulating Face mask
5. Guideline for Import, Sale, Distribution and Use of COVID-19 Self-Test Kits 2022
6. Bhutan National Formulary 2019
7. Bhutan National Formulary for Traditional Medicines 2019
8. Guideline for registration of Biotechnology Products for Human use 
9. Blood and Blood Products Regulation of Bhutan 2016
10. Guide for Import of Hand Sanitizers and Issuance of Import License
11. Emergency Use Authorization procedure and conditions for Deployment of COVID-19 Vaccines
12. Guideline on Pharmacoviglance for Traditional Medicines-Dzongkha version
13. Medical Device Strategy
14. Guideline for Advertisement of Medicinal Products
15. Guideline on Pharmacoviglance for Traditional English-version
16. Guideline on Pharmacoviglance for Veterinary centres
17. National Standards for Blood Transfusion Services
18. Guideline for disposal of Pharmaceutical Waste
19. Guideline for Registration of Biotechnology Products for Veterinary Use
20. Guideline for Registration of API
21. Inspection Guideline
22. Application, Registration fees and Renewal fees
23. Conditions & Documents for ER Registration of Medicinal products
24. Guidance document on Technical Authorization for Manufacture and Regulatory Certifications
25. Guideline for Management and Handling of Defective Medical Products, 2019
26. Sampling Guideline for Pharmaceutical Products and Related Materials, 2019
27. Guidelines for Good Manufacturing Practices of Medical Gases
28. Guidelines for Regulating Human Vaccines
29. Addendum 2021: Guideline for Registration of Medicinal Products 2020
30. Service Delivery Standards