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Drugs (Licensing, Registering and Advertising) Rules, 1976

Topic Serial # Content Case Law
 

PREAMBLE

 
0 PREAMBLE
 

CHAPTER I

 
 

PRELIMINARY

 
1 Short title and commencement
2 Definitions
32 Strike and lock-out
 

CHAPTER II

 
 

MANUFACTURE OF DRUGS FOR SALE

 
3 Types of licences to manufacture drugs
4 Manufacture on more than one set of premises
5 Application for licence to manufacture drugs and fee therefor
6 Duration of a licence to manufacture drugs
7 Certificate of licence to manufacture drugs
8 Central Licensing Board
9 Powers of the Central Licensing Board
10 Procedure of Central Licensing Board
11 Special provisions regarding grant of a licence
12 Cancellation or suspension of licences
13 Renewal of a licence
14 Licensing authority
15 Conditions for grant or renewal of a licence
16 Conditions for the grant or renewal of licence to manufacture drugs by way of formulation
17 Licence to manufacture drugs by way of repacking
18 Condition for the grant or renewal of a licence to manufacture drugs by way of repacking
19 Conditions of licence to manufacture, by way of basic manufacture, semi-basic manufacture formulation and repacking of drugs
20 Additional conditions of licence to manufacture drugs by way of formulation
20 20-A Contract Manufacture
21 Licence to manufacture drugs for experimental purposes
22 Conditions of licence to manufacture drugs for experimental proposes
23 Labeling of drugs manufactured for experimental purposes
 

CHAPTER 3

 
 

REGISTRATION OF DRUGS

 
24 Registration Board
25 Powers of Registration Board
26 Application for registration of drugs and fees thereof
27 Duration of certificate of registration
28 Certificate of registration
29 Procedure for registration
30 Conditions or registration of drug
 

CHAPTER IV

 
 

ADVERTISING OF DRUGS, Etc

 
31 Conditions for Advertising
32 Sampling of drugs
33 Expenditure on advertisement
34 Substances required to be prescribed under Section 24
35 Retailer's discount
 

SCHEDULE A

 
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