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

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

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

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

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

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

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

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

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

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

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

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

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

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14. The NPPA was established in the year:

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

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16. The NPPA operates under the provisions of the:

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

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

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

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

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

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23. FSSAI collaborates with various stakeholders including:

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24. FSSAI has the power to:

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

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

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

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

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

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

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

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

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8. The Poison Act 1919 requires the licensing of:

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9. The Poison Act 1919 empowers the government to:

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10. FSSAI was established in the year:

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11. The primary objective of FSSAI is to:

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12. FSSAI is responsible for setting standards for:

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

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

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

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16. Animal welfare board is established by______ .

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17. Which country enacted the Poison Act in 1919?

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

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

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

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

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22. FSSAI is the regulatory authority responsible for:

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23. FSSAI operates under the jurisdiction of the:

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

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

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

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

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

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

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7. Which one of the following is exempted advertisement.

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

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10. Taking part in the publication of advertisement means_

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

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

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

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

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

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19. Which of the following is the magic remedy.

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

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

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

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

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

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

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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. Natural law theory is based on the belief that:

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

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

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

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

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

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8. The sociological school of jurisprudence focuses on:

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9. CDRI is located at

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

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

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12. Legal realism is a legal theory that:

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

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14. The Pharmacy Act-1948 in India regulates:

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15. ___________ is maintained by Central Council

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16. The concept of legal positivism was developed by:

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

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

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

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20. Legal formalism is a theory that emphasizes:

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

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22. Legal positivism emphasizes:

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23. Jurisprudence is the study of:

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

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

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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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