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Chapter 8 - Pharmaceutical Legislation

Total questions: 15

Worksheet time: 15mins

Name
Class
Date
1.

Poison Act _______

a)

1956

b)

1952

c)

1957

d)

1984

2.

Sales of Drug Act _______

a)

1957

b)

1952

c)

1956

d)

1984

3.

Control of Drugs & Cosmetics Regulation _______

a)

1957

b)

1952

c)

1956

d)

1984

4.

Advertisement Act (Medicine) _______

a)

1957

b)

1952

c)

1956

d)

1984

5.

In the Poison Act 1952, clearly states about importing, possession, compounding, storage, and use of poison

a)

TRUE

b)

FALSE

6.

In the Poison Act 1952, clearly define poison to be any substance that is specified in the Second Schedule.

a)

TRUE

b)

FALSE

7.

In the Poison Act 1952, clearly states any "Controlled Medicine" can be sold or supplied by Pharmacist Assistant and Pharmacist

a)

TRUE

b)

FALSE

8.

In the Poison Act 1952, any product that contains poison listed in the First Schedule known as "Controlled Medicine"

a)

TRUE

b)

FALSE

9.

In the Poison Act 1952, any product that contains non-poison known as over-the-counter

a)

TRUE

b)

FALSE

10.

In the Poison Act 1952, any over-the-counter products also known as __________

a)

Scheduled Poison

b)

Non-scheduled Poison

11.

In the Poison Act 1952, any "Controlled Medicine" products also known as __________

a)

Scheduled Poison

b)

Non-scheduled Poison

12.

In the Sale of Drug Act 1952, clearly states the procedures for any marketed drug whether produced locally or imported

a)

TRUE

b)

FALSE

13.

In the Sale of Drug Act 1952, the term "drug" refers to any substance, product, article to be used on humans only

a)

TRUE

b)

FALSE

14.

In the Sale of Drug Act 1952, the term "drug" refers to any substance, product, article to be used on humans or animals for medicinal purpose

a)

TRUE

b)

FALSE

15.

Choose TWO (2) products to be registered with the Ministry of Health under Control of Drugs & Cosmetics Regulation 1984

a)

Traditional medicine

b)

Cosmetic products

c)

Farm products

d)

Machinery parts