JNTU
JNTU B.Pharmacy IV PHARMACEUTICAL JURISPRUDENCE Previous Question Paper (August/September - 2023 - R17)
Note: i) Question paper consists of Part A, Part B. ii) Part A is compulsory, which carries 25 marks. In Part A, answer all questions. iii) In Part B, Answer any one question from each unit. Each question carries 10 marks and may have a, b as sub questions.
PART A
Define allopathic drug.
Answer
An allopathic drug is defined under the Drugs and Cosmetics Act as any drug intended to be used for or in the diagnosis, treatment, mitigation, or prevention of any disease or disorder in human beings or animals, other than those belonging to the homeopathic, ayurvedic, siddha, or unani systems of medicine.
Write a note on offences and penalties.
Answer
Offences and penalties under the Drugs and Cosmetics Act are categorized based on the severity of the violation. Manufacturing or selling adulterated or spurious drugs can lead to imprisonment ranging from 3 years to life imprisonment and fines not less than 5 lakh rupees. For minor contraventions, such as failure to maintain records or labeling errors, penalties include imprisonment up to 1 year or fines, depending on the specific section violated.
Give the specimen label for Schedule X drug.
Answer
Sign in to view the complete answer paper.
Give the qualifications of Government Analyst.
Answer
Sign in to view the complete answer paper.
Define manufactured drugs and opium derivative.
Answer
Sign in to view the complete answer paper.
Write about sampling procedure for manufacture outside bond.
Answer
Sign in to view the complete answer paper.
Write the objectives of controlling the prices of drugs.
Answer
Sign in to view the complete answer paper.
Write the exemptions for Drugs and Magic Remedies Act.
Answer
Sign in to view the complete answer paper.
Define trade mark and copy right.
Answer
Sign in to view the complete answer paper.
What are the objectives of Drugs Enquiry Committee?
Answer
Sign in to view the complete answer paper.
PART B
Give the conditions for grant of license for manufacture of Schedule C and C1 drugs.
Answer
Sign in to view the complete answer paper.
Write about loan licenses and repacking licenses.
Answer
Sign in to view the complete answer paper.
Write about whole sale and retail sale of drugs.
Answer
Sign in to view the complete answer paper.
Give the qualifications and responsibilities of Drugs Inspector. Explain the sampling procedure to be followed by Drugs Inspector.
Answer
Sign in to view the complete answer paper.
Differentiate between inside and outside bond manufacturing. Explain the procedure for obtaining spirit and its handling for these operations.
Answer
Sign in to view the complete answer paper.
Write the salient features of Narcotic Drugs and Psychotropic Substances Act. What are offences and penalties under this act?
Answer
Sign in to view the complete answer paper.
Write about permitted and prohibited advertisements under Drugs and Magic Remedies Act. Explain its execution.
Answer
Sign in to view the complete answer paper.
Institutional Animal Ethical Committee
Answer
Sign in to view the complete answer paper.
Fixation or retail price of formulation.
Answer
Sign in to view the complete answer paper.
Explain the ethical handling of prescription by pharmacist.
Answer
Sign in to view the complete answer paper.
What are the ethics to be followed by Pharmacist in relation to medical profession?
Answer
Sign in to view the complete answer paper.
Mudaliar Committee
Answer
Sign in to view the complete answer paper.
Pharmacist Oath
Answer
Sign in to view the complete answer paper.