Organizer : Asian College of Pharmacy, Udaipur association with the Indian Drug Manufacturing Association Gujarat State Board and Heltreich Institute for Professional Studies

About the Academic

The Indian Drug Manufacturers’ Association has initiated a plan, under the guidance from Ministry of Health & Family Welfare and Ministry of Chemicals and Fertilisers, to celebrate the first ever “National Current Good Manufacturing Practices Day” (National cGMP Day) on October 10th, 2023. The “National cGMP Day” idea was conceived at the Centre for cGMP, Manipal College of Pharmaceutical Sciences, Manipal and we sincerely propose to celebrate this day every year as National cGMP Day.

This year the entire nation is celebrating Azadi Ka Amrit Mahotsav. On this momentous occasion, it is planned to initiate the practice of celebrating “National cGMP Day”, on 10th October 2023. Quality has no substitute, especially in the Pharmaceutical Industry. cGMP forms the backbone of pharmaceutical manufacturing operations and helps the manufacturers to prevent non-conformances, thereby protecting the Quality of medicinal products. This day shall be dedicated to raising awareness about cGMP and its significance to academia and the entire industry.

“National Current Good Manufacturing Practices Day” 2023

About the Quiz

• Start Date : 10 October 2023
• Free Participates
• Each Participant will be provided E-certificate
• All students, Academician as well as Industrial staff Anyone Can Apply
• Limited time quizzes

Apply Link

Contact Number: 9214365426,

Email: apcudaipur19@gmail.com

 

100% Correct Answers Available Here

1. What is the full form of cGMP
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Good manufacturing practices
Current good manufacturing practices
Covered good manufacturing practices
all

2.  Select the right statement
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Qualification is the part of validation
Validation is part of qualification
Both are different to each other
None of these

3.   What GMP is important
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a. To manufacture consistent quality products
b. To prevent the material for contamination and cross contamination
c. Reduce Rejects/Recalls.
d. All the above

4.    HVAC system comprises of
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a. Air handling Unit
b. Air Conditioners
c. Exhaust system
d. All the above

5.    What is the full form of QC
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a. Quality control
b. Quality contamination
c. Quality conformance
d. None of the above

6.     Personnel must wash their hands thoroughly every time
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a. After returning from breaks and lunches
b. When returning from the rest rooms
c. When entering into the manufacturing area.
d. All the above

7.     Which standard of ISO is applicable for clean room classification
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14644-1
14644-2
14644-3
14644-4

8.      How many principles of GMP
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9
8
10
7

9.       What are the functions of Quality Control lab
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a. Sampling of material
b. Testing of material
c. Documentation
d. All the above

10.        The differential pressure between areas of different class shall be at least:
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a. Min 15 Pascal
b. Min 1.5 mm water gauge
c. Both are same
d. None of the above

11.      Purified water is used in the preparation of
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All non-parenteral preparation/formulation
All parenteral preparation/formulation
In all drugs
All the above

12.      What is the full form of SOP
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Standard operating procedure
Site operating procedure
Standard operating plan
Site operating plan

13.     How many particles of 0.5-5.0 micron allowed at rest in class A.
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0
3500
350000
3500000

14.      Water for Injection is used in the preparation of
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Parenteral and other preparations
For cleaning of parenteral product-contact components
Both of the above
None of the above

15.      What is the limit for microbial count defined for purified water
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100u/ ml
1000 cfu/ ml
10 cfu/ ml
Option 4

16.       Which of the following are guidelines for GMP
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a. Schedule-M
b. ICH-Q7
c. 21 CFR part 210
d. All the above

17.       What is the size of Vent filter used on water storage tank
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0.2 micron
0.3 micron
0.4 micron
0.5 micron

18.       What are the GMP documents
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SOP
Specification
Master formula record
All the above

19.  Which guideline is used for testing of potable water
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BIS 10500: 2012
BIS 15500: 2012
BIS 10520: 2012
BIS 10510: 2012

20.  What is the size of HEPA filter
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0.2 micron
0.3 micron
0.4 micron
0.5 micron

21.  Which schedule is applicable for GMP
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a. Schedule-L
b. Schedule-M
c. Schedule- U
d. None of the above

22.   What is the order of qualification
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PQ, DQ, IQ, OQ
DQ, IQ, OQ, PQ
OQ, PQ , DQ, IQ
IQ, OQ, PQ, DQ

23.    Who is the National president of IDMA
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Mr. Mahesh H Doshi
Mr.Daara B. Pate
Dr. Viranchi Shah
NONE OF ALL ABOVE

24.     Centre for cGMP is located at
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Delhi
Mumbai
Manipal
Chennai

25. If a manufacturing company does not follow the cGMP Regulations then
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Drug manufactured by that company will be called adulterated
no action will be taken ,if drug is safe
Company will be closed instantly
it means that there is necessarily something wrong with drug