Medicines and Related Substances Act, 1965 - General Regulations 2017.

These Regulations deal with the following main points (i) Supply and Registration, detailing the conditions for the supply of medicines, including therapeutic equivalence, compounding, and importation, as well as the registration process for medicines; (ii) Permits and Authorizations, specifyinf the requirements for obtaining permits and licenses for dispensing, manufacturing, importing, and exporting medicines; (iii) Management and Control, including guidelines for the management of medicines, such as prescription particulars, control of medicines in hospitals, and the destruction of medicines or substances.