The Drugs Control Administration, Telangana vide its Circular dated 9th April 2020 has permitted the manufacture of industrial oxygen in order to facilitate the sufficient supply of oxygen for medical use.
The Manufacturer shall follow the below mentioned terms and conditions:
- The permission to manufacture oxygen shall be given only to the manufacturers who has registered with Department of Industries of the State.
- An application in Form 24 of the Drugs and Cosmetics Act, 1940 (“Act”) along with requisite fees and other required documents have to be filed with the Licensing Authority.
- An undertaking has to be submitted to manufacture medical oxygen in compliance with the standards prescribed in Indian Pharmacopia and labeling requirements as per the Act.
- The manufacturer shall use standardized quality materials only and shall supply the finished products at a price which must not exceed the limit fixed by the Central Government or the state Government of Telangana.
- The manufacturing unit must further keep proper records of the manufacturing and supply of the materials suggested by the Drug Inspector in prescribed formats which will be subject to verification at all times.
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