Pharmaceutical Regulations Quiz

Pharmaceutical Regulations Quiz

Professional Development

10 Qs

quiz-placeholder

Similar activities

M7.20 Maintenance Procedures Cat B1 & B2 V7.01

M7.20 Maintenance Procedures Cat B1 & B2 V7.01

Professional Development

15 Qs

anticancer

anticancer

Professional Development

10 Qs

Federal Requirements for Haz and Non-Haz Medications

Federal Requirements for Haz and Non-Haz Medications

12th Grade - Professional Development

13 Qs

EMWP Role Study Quiz

EMWP Role Study Quiz

Professional Development

10 Qs

Monitoring Work Quiz PT7

Monitoring Work Quiz PT7

Professional Development

10 Qs

Quiz PRODUCTION (Guyub)

Quiz PRODUCTION (Guyub)

Professional Development

10 Qs

APS Monthly Game - July

APS Monthly Game - July

Professional Development

15 Qs

Pharmaceutical Regulations Quiz

Pharmaceutical Regulations Quiz

Assessment

Quiz

Other

Professional Development

Hard

Created by

Tejashri Shinde

FREE Resource

10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Schedule G drugs must carry which warning on the label?

Sold by prescription only

Caution: To be sold by licensed chemist only

Caution: It is dangerous to take this preparation except under medical supervision

For external use only

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What symbol must appear on the label of a Schedule H drug?

NRX

OTC

C+

Rx

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What does NRX indicate on a drug label?

Schedule G drug

Over-the-counter drug

Narcotic and psychotropic substance under Schedule H

Non-registered drug

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the primary aim of Schedule M?

Licensing retail pharmacists

Rules for advertisement of drugs

Good Manufacturing Practices (GMP) for drugs

Pricing of medicines

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the minimum area required for tablet manufacturing as per Schedule M?

50 sq. mt.

20 sq. mt.

10 sq. mt.

30 sq. mt.

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is covered under Schedule T of the Act?

Cosmetics manufacturing

Blood products

Ayurvedic, Siddha and Unani medicines manufacturing requirements

Homeopathy formulations

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What information must be included in manufacturing records as per Schedule U1?

Price details

Details of advertising expenses

Serial number, ingredients, duration and conditions of manufacturing process

Only expiry date and batch number

Create a free account and access millions of resources

Create resources
Host any resource
Get auto-graded reports
or continue with
Microsoft
Apple
Others
By signing up, you agree to our Terms of Service & Privacy Policy
Already have an account?