Drugs and Cosmetics Act, 1940 with The Drugs and Cosmetics Rules, 1945

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Description
•    The Drugs and Cosmetics Rules, 1945
as amended by
•    The Drugs and Cosmetics (Sixth Amendment) Rules, 2016
(G.S.R. 897 (E), dated 21-9-2016)
•  The Drugs (Control) Act, 1950, (26 of 1950)
•    The Cost Accounting Records (Bulk Drugs) Rules, 1974
•    Notifications with State Amendments
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Contents
The Drugs and Cosmetic Act, 1940
Chapter I - Introductory
Sec. 1 - 4
Chapter II - The Drugs Technical Advisory Board, The Central Drugs Laboratory
and the Drugs Consultative Committee
Sec. 5 - 7A
Chapter III - Import of Drugs and Cosmetics
Sec. 8 - 15
Chapter IV - Manufacture, Sale and Distribution of Drugs and Cosmetics
Sec. 16-33A
Chapter IV A - Provisions Relating to Ayurvedic, Siddha and Unnani Drugs
Sec. 33B- 33O
Chapter V - Miscellaneous
Sec. 33P - 38
The Drugs and Cosmetics Rules, 1945
Part I : Preliminary
Part II : The Central Drugs Laboratory
Part III :
Part IV : Import and Registration
Part V : Government Analysts, Inspectors, Licensing Authorities and Controlling Autohrities
Part VI : Sale of Drugs othr than Homoeopathic Medicines
Part VIA : Sale of Homoeopathic Medicines
Part VII : Manufacture for sale or for distribution of Drugs other than Homoeopathic Medicines
Part VII A: Manufacture for sale or for Distributon of Homoeopathic Medicines
Part VIII : Manufacture for Examination, Test or Analysis
Part IX  : Labelling and Packing of Drugs other than Homoeopathic Medicines
Part X : Special provisions relating to Biological and Other Special Products
Part XA : Import or Manufacture of new Drug for Clinical Trials or Marketing
Part XB : Requirements for the collection, storate, processing and distribution of wole
                Human Blood, Human Manufacture of Blood Products
Part XI : Exemptions
Part XII : Standards
Part XIII : Import and Registration of Cosmetics
Part XIV : Manufacture of Cosmetic for sale or for Distribution
Part XV : Labelling, Packing and Standards of Cosmetics
Part XV A : Approval of Institutions for carrying out tests on Drugs,
Cosmetics and Raw materials use in their manufactgure on
behalf of liucensees for manufacture for sale of Drugs/cosmetics
Part XVI : Manufacture for sale of Ayurvedic (including  sidha) or Unani Drugs
Part XVI A : Approval of institutions for carrying out tests on Ayurvedic
Sidha and Unani Drugs and Raw Materials used in their manufacture on
behalf of licensees for manufacture for sale of Ayurvedic, siddha and Unani Drugs
Part XVII : Labelling, Packing and Limit of Alcohol in Ayurvedic (including Sidha) or Unani Drugs
Part XVIII : Government Analysts and  Inspectors for Ayurvedic (including Sidha) or Unani Drugs
Part XIX : Standards of Ayurvedic Sidha and Unani Drugs
Schedule A
Form 1 - 50
Schedule B - Schedule Y
The Drugs (Control) Act, 1950
Sections 1 - 20
The Cost Accounting Records (Bulk Drugs) Rules, 1974
Rule 1 - 12
Notifications
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