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Pharmacy Law and Ethics Quiz

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Pharmacy Law and Ethics Quiz (Part-1) :
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Pharmacy Law and Ethics Quiz (Part-1)

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1. Pharmaceutical representatives are expected to adhere to the principles of the Code of Pharmaceutical Ethics during their interactions with healthcare professionals, including:

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2. The Food Safety and Standards Act was passed in the year:

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3. The Code of Pharmaceutical Ethics requires pharmaceutical companies to provide accurate and balanced information about their products, thereby promoting:

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4. The Code of Pharmaceutical Ethics encourages the reporting of adverse events or side effects associated with pharmaceutical products to:

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5. The mechanism used by the NPPA to regulate prices is known as:

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6. The Code of Pharmaceutical Ethics is typically developed and enforced by:

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7. The Code of Pharmaceutical Ethics promotes compliance with relevant __________ regulations and guidelines.

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8. The primary role of the NPPA is to regulate the prices of:

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9. The NPPA operates under the provisions of the:

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10. The Code of Pharmaceutical Ethics discourages the promotion of off-label drug uses, which refers to:

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11. The NPPA has the power to impose penalties on pharmaceutical companies for:

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12. The Code of Pharmaceutical Ethics emphasizes the importance of conducting __________ research to ensure the safety and efficacy of pharmaceutical products.

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13. The NPPA is responsible for fixing the prices of pharmaceutical products based on:

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14. FSSAI collaborates with various stakeholders including:

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15. The NPPA was established in the year:

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16. The chairperson of the NPPA is appointed by the:

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17. The Code of Pharmaceutical Ethics emphasizes the importance of:

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18. The NPPA has the authority to monitor and enforce compliance with pricing regulations by conducting:

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19. The Code of Pharmaceutical Ethics provides guidelines for the ethical conduct of:

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20. The Code of Pharmaceutical Ethics emphasizes the importance of respecting the __________ rights of patients.

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21. FSSAI has the power to:

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22. FSSAI operates a system of __________ to ensure compliance with food safety standards.

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23. The National Pharmaceutical Pricing Authority (NPPA) is an organization under the purview of:

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24. Food businesses in India are required to obtain a/an __________ from FSSAI.

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25. The NPPA's role extends beyond price regulation and includes activities such as:

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Pharmacy Law and Ethics Quiz (Part-2) :
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Pharmacy Law and Ethics Quiz (Part-2)

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1. FSSAI is the regulatory authority responsible for:

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2. The Prevention of Cruelty to Animals Act, 1960, makes it mandatory to obtain a license for the ________________ of performing animals.

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3. The Act includes provisions for the punishment of offenders involved in animal cruelty, with penalties that may include:

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4. The regulatory body established under the Prevention of Cruelty to Animals Act, 1960, is called the:

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5. The Act provides for the establishment of ________________ to prevent cruelty to animals and promote animal welfare.

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6. FSSAI is responsible for setting standards for:

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7. The Poison Act 1919 requires the licensing of:

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8. The Prevention of Cruelty to Animals Act, 1960, in India, aims to:

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9. The Poison Act 1919 empowers the government to:

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10. Which country enacted the Poison Act in 1919?

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11. The Poison Act 1919 established a list of substances classified as:

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12. The possession of poisons without a license under the Poison Act 1919 is considered:

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13. The Poison Act 1919 was primarily aimed at regulating the:

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14. The rule of Prevention of Cruelty to Animals Act was passed in _____

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15. The Poison Act 1919 was introduced to address concerns related to:

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16. The Poison Act 1919 was amended multiple times. Which year saw a significant amendment to the act in India?

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17. FSSAI was established in the year:

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18. Animal welfare board is established by______ .

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19. The Poison Act 1919 provides exemptions for certain categories of individuals, such as:

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20. The primary objective of FSSAI is to:

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21. According to The Prevention of Cruelty to Animals Act, 1960 Animal means any living creature except______.

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22. Which of the following is NOT a requirement under the Poison Act 1919?

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23. FSSAI operates under the jurisdiction of the:

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24. The Prevention of Cruelty to Animals Act, 1960, prohibits acts of cruelty towards:

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25. The primary objective of the Prevention of Cruelty to Animals Act, 1960, is to:

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Pharmacy Law and Ethics Quiz (Part-3) :
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Pharmacy Law and Ethics Quiz (Part-3)

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1. The primary objective of the Narcotic Drugs and Psychotropic Substances Act, 1985, is to:

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2. Which schedule of the Narcotic Drugs and Psychotropic Substances Act, 1985, includes substances like heroin and cocaine?

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3. The Narcotic Drugs and Psychotropic Substances Act, 1985, classifies drugs into how many schedules?

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4. The Narcotic Drugs and Psychotropic Substances Act, 1985, allows for the establishment of _______ for the treatment and rehabilitation of drug addicts.

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5. Which schedule of the Drugs and Magic Remedies Rules, 1955, specifies the list of diseases or ailments for which no advertisement can be made?

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6. The primary objective of the Drugs and Magic Remedies Act, 1954, is to:

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7. Advertisement means any _______, circular, label, wrapper or any other document made orally or by transmitting ______ sound or smoke.

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8. Which one of the following is exempted advertisement.

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9. The punishment for illegal possession of a small quantity of a narcotic drug or psychotropic substance under the Narcotic Drugs and Psychotropic Substances Act, 1985, is:

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10. The Drugs and Cosmetics Act requires drug manufacturers to obtain a ________________ before producing and selling drugs in India.

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11. The Committee that advises the DTAB and various governments on issues related to the uniform functioning of the D & C Act throughout the country is:

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12. The Drugs and Cosmetics Act empowers the CDSCO to regulate and approve:

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13. Which of the following is the magic remedy.

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14. Advertisement made by the company for the treatment of rheumatism, is permitted by Government for six months and if the company is making advertisement after this specified period, then it will be advertisement.

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15. The Drug and Magic Remedies (Objectionable Advertisement) Rules came into force in the year

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16. The regulatory body established under the Narcotic Drugs and Psychotropic Substances Act, 1985, is called the:

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17. The Narcotic Drugs and Psychotropic Substances Act, 1985, in India, aims to:

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18. The Drugs and Cosmetics Act defines “cosmetic” as any substance intended to be applied to the:

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19. Taking part in the publication of advertisement means_

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20. The Drugs and Cosmetics Rules, 1945, mandate the labelling of drugs and cosmetics with information such as:

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21. Publication of the advertisement is prohibited that refer to the use of any drug for the treatment of

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22. Which authority is competent under the Drugs and Magic Remedies (Objectionable Advertisement) Act, 1954 to frame rules for carrying the purpose of the act?

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23. The Narcotic Drugs and Psychotropic Substances Act, 1985, provides special provisions for the control of _____________.

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24. The Narcotic Drugs and Psychotropic Substances Rules, 1985, provide guidelines for:

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25. The Narcotic Drugs and Psychotropic Substances Rules, 1985, specify the procedure for ________________ of seized drugs and psychotropic substances.

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Pharmacy Law and Ethics Quiz (Part-4) :
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Pharmacy Law and Ethics Quiz (Part-4)

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1. The Pharmacy Act-1948 establishes which regulatory body in India?

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2. The Practice Regulations-2015 require pharmacists to maintain records of:

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3. Legal formalism is a theory that emphasizes:

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4. Schedule U, of D & C Act and Rules deals with

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5. The Pharmacy Act-1948 in India regulates:

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6. ___________ is maintained by Central Council

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7. Which legal theory emphasizes the importance of individual rights and freedoms?

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8. Jurisprudence is the study of:

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9. If a drug is so coloured, coated or polished that it would appear, of better or greater therapeutic value than it really has is known as:

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10. The concept of legal positivism was developed by:

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11. The primary objective of the Drugs and Cosmetics Act, 1940, is to:

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12. Legal realism is a legal theory that:

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13. The Practice Regulations-2015 under The Pharmacy Act-1948 provides guidelines for:

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14. The primary objective of The Pharmacy Act-1948 is to:

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15. The Practice Regulations-2015 require pharmacists to undergo continuing education to:

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16. The sociological school of jurisprudence focuses on:

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17. According to The Pharmacy Act-1948, a registered pharmacist is authorized to:

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18. Following of which is the ex-officio member of PCI?

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19. CDRI is located at

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20. Legal positivism emphasizes:

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21. Natural law theory is based on the belief that:

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22. The critical legal studies movement criticizes the law for:

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23. The number of hours of practical training for a registered pharmacist is:

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24. The regulatory body established under the Drugs and Cosmetics Act, 1940, is called the:

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25. Which of the following is NOT a source of law?

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Pharmacy Law and Ethics Quiz – 
Get ready to navigate the essential legal and ethical frameworks in pharmacy with our Pharmacy Law and Ethics Quiz! Featuring 100 MCQs organized into 4 sets of 25 questions each, this quiz covers critical topics like federal and state regulations, prescription laws, and the ethical responsibilities of pharmacists. You’ll tackle real-world scenarios that challenge your understanding of patient confidentiality, informed consent, and professional conduct. Each question is designed to provoke thought and discussion, helping you to grasp not only the laws but also the ethical principles that guide pharmacy practice. This preparation will ensure you’re well-equipped for the D Pharma Exit Exam (DPEE) and ready to make responsible decisions in your future career.


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