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Rule 11, Inter-Services Organisations (Command, Control and Discipline) Act Rules, 2025 [S2C-6FY]

As at 7 September 2026. In force from 23 February 2025.

In Inter-Services Organisations (Command, Control and Discipline) Act Rules, 2025 [R10-AYK]. This text from 23 February 2025. No other text held.

Synthetic. This instrument and its words are generated by the register.

Cite: Rule 11, Inter-Services Organisations (Command, Control and Discipline) Act Rules, 2025 [S2C-6FY]. Machine: S2C-6FY.

11. Procedure for the manufacture of drugs.—(1) Every manufacturer shall, before undertaking the manufacture of drugs, intimate the Licensing Authority in writing, specifying the drug concerned and the period for which it is proposed to be undertaken. (2) The Licensing Authority may, within thirty days of the receipt of the intimation, require the person to furnish such further particulars as it considers necessary.

Defined terms in this text (3)

drug: Section 2, Epidemic Disease Act, 1897 [S159N1] (In this Act, unless the context otherwise requires,—): "drug" includes all medicines for internal or external use of human beings or animals and all substances intended to be used for or in the diagnosis, treatment, mitigation or prevention of any disease or disorder in human beings or animals

drug: Section 2, Indian Nursing Council Act, 1947 [S193WH] (In this Act, unless the context otherwise requires,—): "drug" includes all medicines for internal or external use of human beings or animals and all substances intended to be used for or in the diagnosis, treatment, mitigation or prevention of any disease or disorder in human beings or animals

drug: Section 2, Pharmacy Act, 1948 [S19FD3] (In this Act, unless the context otherwise requires,—): "drug" includes all medicines for internal or external use of human beings or animals and all substances intended to be used for or in the diagnosis, treatment, mitigation or prevention of any disease or disorder in human beings or animals

drug: 17 more definitions.

Licensing Authority: Section 2, Maharashtra Nursing Homes Registration Act, 1949 [S2E6ZB] (In this Act, unless the context otherwise requires,—): "Licensing Authority" means the authority appointed under this Act to grant licences under this Act

Licensing Authority: Section 2, Tamil Nadu Private Clinical Establishments (Regulation) Act, 1997 [S2K6PA] (In this Act, unless the context otherwise requires,—): "Licensing Authority" means the authority appointed under this Act to grant licences under this Act

Licensing Authority: Section 2, Karnataka Private Medical Establishments Act, 2007 [S2MFKW] (In this Act, unless the context otherwise requires,—): "Licensing Authority" means the authority appointed under this Act to grant licences under this Act

Licensing Authority: 19 more definitions.

manufacture: Section 2, West Bengal Excise Act, 1909 [S2DK2J] (In this Act, unless the context otherwise requires,—): "manufacture" includes every process, whether natural or artificial, by which any excisable article is produced or prepared

manufacture: Section 2, Punjab Excise Act, 1914 [S2DN8Y] (In this Act, unless the context otherwise requires,—): "manufacture" includes every process, whether natural or artificial, by which any excisable article is produced or prepared

manufacture: Section 2, Madhya Pradesh Excise Act, 1915 [S2DQ6A] (In this Act, unless the context otherwise requires,—): "manufacture" includes every process, whether natural or artificial, by which any excisable article is produced or prepared

manufacture: 34 more definitions.

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