Good Manufacturing Practice for Ayurveda, Siddha and Unani drugs ensures that, the pharmaceutical premises, raw materials used for manufacturing , the complete manufacturing processes, the quality control measures adopted and the manufactured drug released for sale are all of acceptable quality as specified in Schedule T of Drugs & Cosmetic Act 1940 & Rules 1945.

The request for GMP certificate in 24E1 form with the proposed standard operative procedures of the firm should be submitted along with the application for Fresh Drug License.