wayground logo

Free Printable Worksheets

Font size

S
M
L
XL
Worksheets

Manuf Quiz 1

Total questions: 15

Worksheet time: 8mins

Name
Class
Date
1.

The making by physical, chemical, biological or any other procedure of any article that meets the definition of drugs

a)

Pharmaceutical Manufacturing

b)

Extemporaneous Compounding

2.

Small scale preparation of drug products

a)

Extemporaneous Compounding

b)

Pharmaceutical Compounding

3.

The complete set of activities to produce a drug comprise production and quality control from dispensing of materials to the release for distribution of the finished product

a)

Extemporaneous compounding

b)

Pharmaceutical Compounding

4.

Part of Quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use.

a)

Good CLINICAL Practices

b)

Good LABORATORY Practices

c)

Good MANUFACTURING Practices

d)

Good DISTRIBUTION Practices

e)

Good DOCUMENTATION Practices

5.

A type of drug establishment in which prescription drugs are being manufactured.

a)

Biologicals Manufacturers

b)

Ethical Manufacturers

c)

Proprietary/Generic Manufacturers

d)

Medicinal Chemical Manufacturers

6.

Type of establishment where produce drugs for other companies

a)

Toll Manufacturers

b)

Vet Manufacturers

c)

Ethical Manufacturers

d)

Biologicals Manufacturers

7.

Imports of exports raw materials, active ingredients or finished products for its own use or for wholesale distribution on whole sale basis

a)

Drug Distributor/Importer/ Exporter

b)

Drug Trader

c)

Drug Wholesaler

d)

Drug Manufacturer

8.

Vaccines, Toxoids, Antisera, Biotech Products are produced by _____________.

a)

Ethical Manufacturers

b)

Biologicals Manufacturers

c)

Proprietary/ Generic Manufacturers –

d)

Medicinal Chemical Manufacturers

9.

Manufacture Active ingredients and recipients

a)

Medicinal Chemical Manufacturers

b)

Toll/Contract Manufacturers

c)

Veterinary Products Manufacturers

d)

Proprietary/ Generic Manufacturers

10.

Registered owner of the drug product but subcontracts toll manufacture of such products to a licensed manufacturer

a)

Drug Manufacturers

b)

Drug Trader

c)

Drug Distributor

d)

Drug Wholesaler

11.

Which regulatory body first introduced cGMP?

a)

World Health Organization (WHO)

b)

Food and Drug Administration (FDA)

12.

Which document governs cGMP standards for drug manufacturing in the Philippines?

a)

Administrative Order No. 43, Series 1999

b)

Republic Act 9711

13.

In the context of cGMP, what does "Good Manufacturing Practices" ensure for pharmaceutical products?

a)

High sales and profitability

b)

Safety, quality, and efficacy

14.

Which of the following is an example of Good Documentation Practices under cGMP?

a)

Using pencils to fill out important records

b)

Ensuring records are complete, accurate, and legible

15.

How does adherence to cGMP help a pharmaceutical company during FDA inspections?

a)

It minimizes the risk of violations and warning letters

b)

It increases the frequency of FDA inspections