National Medicines Regulatory Authority Act, No. 5 of 2015.

This Act establishes the National Medicines Regulatory Authority (Authority) and provides for its functions and powers in respect of medicines and medical devices. Chapter I states the objects of the Authority and contains the composition of the Authority. It lays down the powers and functions of the Authority. Chapter II establishes the National Advisory Committee and its divisions and provides for the National Medicines Quality Assurance Laboratory. Chapter III lays down the functions of the Medicines Regulatory Division of the Authority and provides for the registration and licensing of medicines. Chapter IV controls and regulates all aspects of medical devices. Chapter VI contains provisions in respect of sale, manufacturing, import and pricing of medicines and medical devices. Chapter VII regulates pharmacies and contains powers of authorised officers.