MULTIPLE CHOICE
QUESTIONS
1. The ultimate goal of GMP is …………..
(A).
The manufacturing process is as has been
prescribed to maintain the standards
(B).
Safeguarding the health of the patient
as well as producing good quality medicine
(C).
The manufactured drug which is released
for sale is of acceptable quality
(D).
All
2. The quality control section
shall have minimum ------------- area.
(A).
150 sq feet
(B).
200 sq feet
(C).
250 sq feet
(D).
300 sq feet
3. The premises used for
manufacturing, processing, packaging and labeling will be in conformity with
the provisions of …………………..
(A).
Drugs and Cosmetics Act, 1940
(B).
Factory Act
(C).
Current Good Manufacturing Practices
(D).
All
4. Procedure of ………………….should be
adopted for raw materials wherever necessary.
(A).
WHO guideline
(B).
First in first out
(C).
Standard Storage conditions
(D).
None
5. The finished goods transferred
from the production area after proper packaging shall be stored in the finished
goods stores, marked as ……………….
(A).
Finished Goods Stock
(B).
Quarantine
(C).
Finished Product
(D).
None
6. Records of sale and distribution
of each batch of Ayurveda, Siddha and Unani Drugs shall be maintained up to
--------------- of the exhausting of stock.
(A).
2 Years
(B).
5 Years
(C).
10 Years
(D).
15 Years
7. The manufacturer shall submit
the record related to complaints to the Licensing Authority, once in a period
of ………………..
(A).
3 Months
(B).
6 Months
(C).
9 Months
(D).
12 Months
ANSWERS
|
1 |
D |
2 |
A |
3 |
B |
4 |
B |
|
5 |
B |
6 |
B |
7 |
B |
|
|
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