20226 Pharmacy Law & Ethics MCQ with Answers

Want to prepare for the MSBTE exam? However, you do not have access to sources where you can practice for the exam. Here we are to help you with Pharmacy Law & Ethics MCQ With Answers for the 2nd-year students. We have got the best collection of the most important and frequently repeated multiple-choice questions from the  Pharmacy Law & Ethics Multiple Choice Questions with answers. To make your studies easier and for better practice, we have built a set of 40 multiple-choice questions that can be very helpful for all the D-Pharmacy students.

The following Pharmacy Law & Ethics MCQ Test is the best and perfectly made for the 2nd-year D-Pharmacy students to make themselves ready for the upcoming MSBTE summer exam 2025. Once you prepare for the mock test paper, we have shared Pharmacy Law & Ethics MCQ PDFs at the end for better understanding. It will help you to get confident in the multiple-choice questions and answers given in the test paper.

Pharmacy Law & Ethics Multiple choice Questions with answers

Pharmacy Law & Ethics MCQ with Answers

20226 Pharmacy Law & Ethics Multiple Choice Questions with Answers

1 / 40

1.Which of the following qualifications is required for appointment as a Drug Inspector?

High school certificate

Bachelor’s degree in Pharmacy or Medicine with a specialization in Clinical Pharmacology or Microbiology

Diploma in Pharmacy

Certificate course in pharmaceutical marketing

2 / 40

2.A primary duty of a Drug Inspector in relation to the sale of drugs is to:

Approve new drug registrations

Inspect all licensed drug establishments at least twice a year

Develop drug formulations

Conduct clinical trials

3 / 40

3.With respect to the manufacture of drugs, a Drug Inspector is responsible for:

Marketing the drugs

Inspecting licensed manufacturing premises to ensure compliance with the Act

Training pharmacists

Approving retail pricing

4 / 40

4.Which of the following correctly describes an elected member in the constitution of the Pharmacy Council of India (PCI)?

A member elected from the Central Government only

A teacher from each subject (Pharmaceutical Chemistry, Pharmacy, Pharmacology, Pharmacognosy) on the teaching staff of a recognized university

A registered pharmacist from the State Council

A representative from a pharmaceutical industry association

5 / 40

5.One key function of the PCI is to:

Regulate the pricing of drugs

Appoint inspectors to assess the minimum educational standards in pharmacy institutions

Manufacture pharmaceuticals

Conduct clinical trials

6 / 40

6.In clinical trial phases, Phase I is primarily concerned with:

Establishing therapeutic efficacy in a large patient group

Evaluating safety and side effects in a small group of healthy volunteers

Post-marketing surveillance

Confirmatory testing in multicenter trials

7 / 40

7.Phase II clinical trials are also known as:

Human pharmacology studies

Therapeutic exploratory trials

Post-marketing studies

Dose-ranging studies only

8 / 40

8.Phase IV clinical trials are characterized by:

Initial testing in healthy volunteers

Therapeutic exploratory studies

Confirmatory large-scale trials

Post-marketing surveillance

9 / 40

9.The Central Drug Laboratory (CDL) is primarily tasked with:

Regulating pharmacy education

Analyzing and testing samples of drugs and cosmetics

Licensing drug manufacturing

Approving clinical trial protocols

10 / 40

10.According to the pharmacist’s code of ethics, one important role is to:

Alter prescriptions without consulting the prescriber

Maintain the professional appearance and standards of the pharmacy

Endorse one particular prescriber over others

Dispense drugs without verifying prescriptions

11 / 40

11.Which of the following is an ex-officio member of the Drugs Technical Advisory Board (DTAB)?

A registered pharmacist elected by state councils

The Director-General of Health Services (who acts as chairman)

A nominated representative from the pharmaceutical industry

A teacher from an affiliated college

12 / 40

12.A nominated member of DTAB is selected by:

The State Government

The Central Government

Public vote

The Pharmacy Council of India

13 / 40

13.Which option is NOT an objective of the Drug Price Control Order (DPCO)?

Ensuring essential medicines are available at reasonable prices

Supporting industry innovation and competition

Maximizing profit margins for manufacturers

Promoting shared economic growth

14 / 40

14.The formula for calculating the retail price of a drug formulation includes all the following except:

Material cost (M.C.)

Conversion cost (C.C.)

Advertising expense

Excise duty (ED)

15 / 40

15.Under the Drugs and Magic Remedies (DMR) Act, 1954, a “Magic Remedy” refers to:

A scientifically validated medication

A talisman, mantra, or charm claimed to have miraculous powers

A homeopathic drug

An over‐the‐counter analgesic

16 / 40

16.The Biopharmaceutics Classification System (BCS) differentiates drugs based on:

Their therapeutic indications and side effects

Their solubility and permeability characteristics

Their manufacturing cost

Their dosage forms

17 / 40

17.Which principle of law ensures that all individuals are treated equally before the law?

Supremacy of law

Equality before law

Principle of liberty

Predominance of legal spirit

18 / 40

18.Under the Drugs and Cosmetics Act, 1940, a Drug Inspector has the power to:

Issue new drug licenses

Enter and search premises where drug offenses are suspected

Develop new drug formulations

Set retail prices

19 / 40

19.Which of the following operations is directly controlled by the Central Government under the NDPS Act, 1985?

Approval of pharmacy college curricula

Cultivation of opium poppy

Licensing of retail pharmacies

Marketing of over‐the‐counter drugs

20 / 40

20.The required qualification for a Government Analyst includes:

A diploma in computer applications

A graduate or postgraduate degree in medicine, science, pharmacy, or pharmaceutical chemistry

No formal qualification

A certificate in quality control only

21 / 40

21.Which of the following is typically NOT a required document in hospital pharmacy documentation?

Regulatory licenses and registrations

Purchase and sales invoices

Detailed manufacturing processes

Patient medication records

22 / 40

22.The first step in preparing the First Register under the Pharmacy Act, 1948, is the:

Issue of registration certificates

Constitution of a Registration Tribunal

Publication of the register

Appointment of a chief pharmacist

23 / 40

23.When taking drug samples, Form 16 is used by a Drug Inspector to:

Record the inspection findings

Issue a receipt when the price is refused

Approve sample quality

Notify the prescriber

24 / 40

24.A drug is considered “adulterated” if it is:

Prepared, packed, or stored under unsanitary conditions

Manufactured under strict quality controls

Packaged in approved containers

Labeled correctly

25 / 40

25.A “misbranded” drug is defined as one that:

Contains all the correct ingredients

Bears a false or misleading label or claim

Is manufactured using standard methods

Is priced competitively

26 / 40

26.The function of the CDL carried out at the Central Research Institute, Kasauli, involves:

Routine inspection of pharmacies

Testing specific classes of drugs such as vaccines and antigens

Licensing drug inspectors

Conducting preclinical research

27 / 40

27.Schedule N of the Drugs and Cosmetics Rules, 1945, specifies:

A) The procedures for clinical trials

The minimum equipment, premises, and layout requirements for a pharmacy

Drug pricing formulas

Qualifications for drug inspectors

28 / 40

28.An objective of DPCO 2013 is to:

Ensure essential medicines are available at affordable prices

Increase the profit margins of pharmaceutical companies

Reduce competition in the market

Eliminate the need for clinical trials

29 / 40

29.Active Pharmaceutical Ingredients (APIs) are defined as:

Inactive fillers in a drug formulation

Substances that are pharmaceutically active and used as ingredients in drugs

Excipients used solely for tablet binding

Color additives in medication

30 / 40

30.One key difference between law and ethics is that:

Laws are moral guidelines, while ethics are legally enforceable

Laws are compulsory with penalties for non-compliance, whereas ethics are moral principles without legal sanctions

Ethics are written in statute books, whereas laws are not

There is no significant difference

31 / 40

31.In relation to pricing, a pharmacist is expected to:

Set arbitrary high prices for profit maximization

Calculate the retail price using prescribed formulas and ensure fair trade practices

Ignore government regulations

Reduce prices by compromising drug quality

32 / 40

32.The initial step in the new drug development process is:

Preclinical research

Discovery and development

FDA review

Post-market safety monitoring

33 / 40

33.Preclinical research primarily involves:

A) Testing drug safety and toxicity in animal models

Conducting large-scale human trials

Marketing the drug

Post-approval surveillance

34 / 40

34.Large-scale clinical trials to confirm efficacy are typically conducted in:

Phase I

Phase II

Phase III

Phase IV

35 / 40

35.Under the Drugs and Cosmetics Act, 1940, the licence for manufacturing drugs other than those specified in Schedule C, C1, and X is issued in:

Form 20

Form 21

Form 20F

Form 20B

36 / 40

36.“Repacking” of drugs is defined as:

The synthesis of new drug compounds

Breaking bulk drugs into smaller packages and relabeling them for sale

Dispensing drugs at a pharmacy counter

Compounding drugs in a hospital setting

37 / 40

37.A condition for the grant of a repacking licence is that the licensee must:

Maintain an inspection book (e.g., Form 35) to record repacking operations

Ignore quality control tests

Use any available space regardless of hygiene

Repack drugs without supervision

38 / 40

38.Under the NDPS Act, 1985, “illicit traffic” includes:

Regulated import and export of approved drugs

Cultivating opium poppy and unauthorized handling of narcotic drugs

Legitimate transportation of pharmaceuticals

Manufacturing drugs in licensed facilities

39 / 40

39.Under the Drugs and Magic Remedies (OA) Act, 1954, a first conviction for contravention of the Act may result in

Life imprisonment

Imprisonment for six months or a fine or both

A mere warning

Community service only

40 / 40

40.Under the Poison Act, 1919, the State Government regulates:

The marketing of all over‐the‐counter drugs

The sale and possession of specified poisons

Licensing of pharmaceutical manufacturers

Clinical trial protocols

Your score is

The average score is 56%

By Wordpress Quiz plugin

Students also Search for:

Pharmacy Law & Ethics 2nd Year Question papers [View Here]

2nd Year Pharmacy Law & Ethics Answer Paper [View Here]

Pharmacy Law & Ethics Syllabus [View Here]

Pharmacy Law & Ethics MCQ Test

This set of multiple-choice questions has been a great help to all the students who have joined us and practiced these before their MSBTE exams. A key fact for all the students to understand is that a single problem can have various methods of getting a solution; the only thing that matters is that the answer produced must be the same. We have provided the best and correct questions and answers in the Pharmacy Law & Ethics 2nd Year Model Answer Paper PDF. For either of the differences in answers between the PDF and the textbook, you will get the same solution. You have the freedom and flexibility to write the answer as given in the Pharmacy Law & Ethics 2nd Year Model Answer Paper for your upcoming MSBTE exam. You can opt for the best-suited answer that is easier for you and has an important point. Always remember that the important aspect is to get the right answer.

Free Mock Test For competitive exams (View Here)

Pharmacy Adda Social accounts

Stay up-to-date with the latest pharmacy news and updates by following us on Instagram @pharmacyadda.in and Facebook @pharmacyadda.in. We regularly post important updates and announcements to keep you informed. If you have any questions about diploma or engineering courses, feel free to message us on social media—we’re here to help!

Thankyou for Visiting Pharmacy Adda

Pharmacyadda.in is a platform especially built to help students and wants to make studying easier for all who are studying pharmacy. We help and assist all the students by providing a full set of multiple-choice question banks with answers for students presently pursuing their courses in the field of D-Pharmacy, B-Pharmacy, or M-Pharmacy. The sets of given question papers are prepared by the experts who have experience and a great understanding of the exam. It will help you to get familiar with the question paper and its important topics. This MSBTE multiple-choice question paper has been a great help in focusing and achieving the goal with the best preparation.