Topic Serial # |
Content |
Case Law |
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PREAMBLE
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0 |
PREAMBLE
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CHAPTER I
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PRELIMINARY
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1 |
Short title and commencement
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2 |
Definitions
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32 |
Strike and lock-out
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CHAPTER II
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MANUFACTURE OF DRUGS FOR SALE
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3 |
Types of licences to manufacture drugs
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4 |
Manufacture on more than one set of premises
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5 |
Application for licence to manufacture drugs and fee therefor
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6 |
Duration of a licence to manufacture drugs
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7 |
Certificate of licence to manufacture drugs
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8 |
Central Licensing Board
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9 |
Powers of the Central Licensing Board
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10 |
Procedure of Central Licensing Board
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11 |
Special provisions regarding grant of a licence
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12 |
Cancellation or suspension of licences
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13 |
Renewal of a licence
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14 |
Licensing authority
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15 |
Conditions for grant or renewal of a licence
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16 |
Conditions for the grant or renewal of licence to manufacture drugs by way of formulation
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17 |
Licence to manufacture drugs by way of repacking
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18 |
Condition for the grant or renewal of a licence to manufacture drugs by way of repacking
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19 |
Conditions of licence to manufacture, by way of basic manufacture, semi-basic manufacture formulation and repacking of drugs
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20 |
Additional conditions of licence to manufacture drugs by way of formulation
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20 |
20-A Contract Manufacture
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21 |
Licence to manufacture drugs for experimental purposes
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22 |
Conditions of licence to manufacture drugs for experimental proposes
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23 |
Labeling of drugs manufactured for experimental purposes
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CHAPTER 3
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REGISTRATION OF DRUGS
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24 |
Registration Board
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25 |
Powers of Registration Board
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26 |
Application for registration of drugs and fees thereof
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27 |
Duration of certificate of registration
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28 |
Certificate of registration
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29 |
Procedure for registration
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30 |
Conditions or registration of drug
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CHAPTER IV
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ADVERTISING OF DRUGS, Etc
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31 |
Conditions for Advertising
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32 |
Sampling of drugs
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33 |
Expenditure on advertisement
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34 |
Substances required to be prescribed under Section 24
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35 |
Retailer's discount
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SCHEDULE A
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