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THE DRUGS AND COSMETICS ACT,
1940
(Amended in 1995)
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The Drugs and Cosmetics Act is
mainly aimed to regulate the import, manufacture, distribution
and sale of Drugs and Cosmetics, presumably for maintaining
high standards of medical treatment. Substandard medicines
/ drugs may cause severe damage to lives of people. |
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All Medicines (Ayurvedic, Sddha,
and Unani) for internal or external use of human being
or animals and all substances (other than food) intended
to be used for or in the diagnosis, treatment, mitigation
or prevention of any disease or disorder in human beings
or animals including preparation applied on human body
or to destroy insects. |
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The Central or State government
have power to make rules and appoint inspector to control
or inspect any drug or cosmetic for its standardization
and safety which can be tested in the Central or State
Drug laboratory. The Government can prohibit manufacturing,
importing or selling of any drug or cosmetic. Violation
of law by any person or corporate manager or owner is
liable for punishment for a term which may extend to
3-10 years and shall also be liable to fine which could
be five hundred or ten thousand rupee or with both. |
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Drugs and Cosmetic Rules 1995 contains
the list of drugs for which license is required by manufacturer,
importers, and exporters. Recently ’in vitro’
blood groups, sera and in vitro diagnostic devices for
HIV, HBsAg, and HCV are also included in schedule CI.
All imported drugs in indigenous manufacturers have
to register to control over the quality of imported
as well as locally manufacturing kits. |
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Reference |
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Drugs and Cosmetic Rules 1995
vide Gazette Notification – GSR No. 86 (E) A 6/2/02. |
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The Gazette of India. The Drugs
and Cosmetics Act 1940. No. 23 of 1940. |
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