The Directorate General of Drug Administration (DGDA) under the Ministry of Health & Family Welfare, Government of the People's Republic of Bangladesh, is the Drug Regulatory Authority of the country. DGDA supervises and implements all prevailing Drug Regulations in the country and regulates all activities related to import, procurement of raw and packing materials, production and import of finished drugs, export, sales, pricing, etc. of all kinds of medicines including those of Ayurvedic, Unani, Herbal and Homoeopathic systems, drugs and medicines. Besides, a number of Committees, such as Drug Control Committee (DCC), Standing Committee for imports of raw materials and finished drugs, Pricing Committee, and a number of other relevant Committees, which comprise experts of different fields, are there to advise the Licensing Authority and recommend him about matters related to drugs and medicines. Overall, the purpose of this course is to learn about the rules and regulations of Pharmacy practices