Schedule R, R-1 and schedule S||Pharmaeasynotes ||@Pharmacy || Jurisprud...

Schedule 'T'
Requirements (GMP) of factory premises for Ayurvedic, Siddha, Unani drugs. 

For getting a certificate of 'Good Manufacturing Practices' of Ayurveda Siddha- Unani drugs,  

the applicant shall make an application on plain paper,  providing the information on the existing infrastructure of the manufacturing unit, and the licensing authority shall after verification of the requirements as per Schedule T issue the certificate within  a period of 3 months in form 26-E

Schedule 'U'

Manufacturing, raw materials, and analytical record of drugs ðŸ’Š

Lot of the raw materials used for the manufacturing of products and also each batch of the final product and shall maintain records. 

The records or registers shall be retained for a period of 5 years from the date of manufacturing. 

Schedule 'U(1)'

Manufacturing, raw materials, and analytical records of cosmetics

The licensee shall keep records of the details of each batch of cosmetics manufactured by him and of raw materials used therein as per particulars specified in schedule U(1). 

Such records shall be retained for a period of three years. 


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