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Worksheets

Federal Regulatory Agencies & Laws

Total questions: 25

Worksheet time: 13mins

Name
Class
Date
1.

Law that involves cases such as Medical malpractice

a)

State Pharmacy Law

b)

Criminal Law

c)

Tort Law

d)

Federal Pharmacy Law

2.

C-IV scheduled drugs

a)

Benzodiazepines

b)

Nitroglycerin

c)

Testosterone

d)

Generic drugs

3.

A drug which does not require child-safety cap

a)

Testosterone

b)

Pseudophedrine

c)

Nitroglycerin

d)

Benzodiazepines

4.

Male hormone which gave rise to anabolic drugs

a)

Generic drugs

b)

Pseudophedrine

c)

Nitroglycerin

d)

Testosterone

5.

Issue and enforce standards for workplace safety and health

a)

FDA

b)

NIOSH

c)

OSHA

d)

DEA

6.

Ensures the safety and health of America's workers by setting and enforcing standards

a)

SSA

b)

SBOP

c)

JCAHO

d)

OSHA

7.

Evaluates and accredits healthcare institutions

a)

TJC

b)

DEA

c)

CDC

d)

CMEA

8.

Regulates the legal trade of Narcotic and dangerous drugs

a)

SBOP

b)

DEA

c)

OBRA '90

d)

SSA

9.

Agency established by FDCA (Federal Drug Cosmetic Act)

a)

SSA

b)

OSHA

c)

NIOSH

d)

FDA

10.

Required Pharmacists to counsel patients

a)

CDC

b)

OBRA '90

c)

SSA

d)

SBOP

11.

Agency that registers and regulates pharmacy facilities, Pharmacists and Techs

a)

DEA

b)

SBOP

c)

FDA

d)

CMEA

12.

Requirement of prescription to read "Rx only"

a)

Durham-Humphrey Amendment

b)

Affordable Care Act of 2010

c)

Anaboic Steroid Control Act

d)

Medicare Modernization Act

13.

Requires mfg to show report to FDA on safety of a drug

a)

Poison Prevention Packaging Act

b)

Controlled Substances Act

c)

Kefauver-Harris Amendment

d)

Drug Listing Act

14.

Requirement of childproof/child safety caps

a)

Poison Prevention Packaging Act

b)

Medical Device Amendment

c)

Orphan Drug Act

d)

Drug Listing Act

15.

Act which required mfg to register their products with FDA

a)

Medicare Modernization Act

b)

Controlled Substance Act

c)

Drug Listing Act

d)

Federal Pharmacy Law

16.

Drug price competition and patent term restoration was put in place in regards to ________________

a)

Medical Device Amendment

b)

Anabolic Steroid Control Act

c)

Medicare Modernization Act

d)

Generic Drugs

17.

Enacted to ensure patient confidentiality and privacy

a)

Durham-Humphrey Amendment

b)

Federal Pharmacy Law

c)

HIPAA

d)

Orphan Drug Act

18.

Focuses on development of drugs for rare diseases (those that affect 200,000 people or less)

a)

Kefauver-Harris Amendment

b)

Orphan Drug Act

c)

Drug Listing Act

d)

Affordable Care Act

19.

Which law allows a pharmacist to accept a telephoned prescription from a Physician's office?

a)

Pure Food and Drug Act of 1906

b)

Food, Drug and Cosmetic Act of 1938

c)

Durham-Humphrey Act of 1950

d)

Kefauver-Harris Act of 1962

20.

The first of a series of significant consumer protection laws which was enacted by Congress in the 20th century and led to the creation of the Food and Drug Administration

a)

Pure Food and Drug Act of 1906

b)

Food, Drug and Cosmetic Act of 1938

c)

Durham-Humphrey Act of 1950

d)

Kefauver-Harris Act of 1962

21.

The pharmacist fails to place an RX label on the medication container. Which law is being broken?

a)

Pure Food Drug Act of 1906

b)

Food, Drug and Cosmetic Act of 1938

c)

Durham-Humphrey Act of 1950

d)

Kefauver-Harris Act of 1962

22.

An employee injures his back while lifting a heavy box of medication in the pharmacy. What law allows the employee to collect damages from the employer?

a)

Kefauver-Harris Act

b)

Omnibus Budget Reconciliation Act of 1987

c)

Poison Prevention Act of 1970

d)

Occupational Safety and Health Act of 1970

23.

Which Act requires companies with 20 or more employees to give workers and their families COBRA coverage to extend health insurance

a)

Occupational Safety and Health Act of 1970

b)

Omnibus Budget Reconciliation Act of 1987

c)

Poison Prevention Act of 1970

d)

Kefauver-Harris Act of 1962

24.

An amendment to the Federal Food, Drug, and Cosmetic Act. introduced a requirement for drug manufacturers to provide proof of the effectiveness and safety of their drugs before approval, required drug advertising to disclose accurate information about side effects, and stopped cheap generic drugs being marketed as expensive drugs under new trade names as new "breakthrough" medications.

a)

Kefauver-Harris Act of 1962

b)

Pure Food and Drug Act of 1906

c)

Durham-Humphrey Act of 1950

d)

Poison Control Act

25.

Which law requires that a manufacturer provide an SDS to a pharmacy for products that are combustible, flammable, or can cause injury to an individual if he or she comes into contact with the substance?

a)

Kefauver-Harris Act of 1962

b)

Controlled Substances Act of 1970

c)

Occupational Safety Act of 1970

d)

Poison Prevention Act of 1970