>
Pharmaceutical Jurisprudence
List of top Pharmaceutical Jurisprudence Questions
Who has the power to fix the ceiling price of scheduled formulations:
GPAT - 2024
GPAT
Pharmaceutical Jurisprudence
Standard institutions and regulatory authorities
The term of a patent granted under Indian Patent’s Act is:
GPAT - 2024
GPAT
Pharmaceutical Jurisprudence
Standard institutions and regulatory authorities
Schedule T of Drugs and Cosmetics Rules, 1945 deals with:
GPAT - 2024
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
The number of persons elected as the member of the Pharmacy Council of India from the teaching profession is:
GPAT - 2023
GPAT
Pharmaceutical Jurisprudence
Standard institutions and regulatory authorities
Requirement of factory premises for the manufacture of cosmetics are mentioned in the Drugs and Cosmetics Rules, 1945 under:
GPAT - 2023
GPAT
Pharmaceutical Jurisprudence
Factory Act
Which of the following ICH Hannonized Tripartite Guidelines related to stability, provides the general requirements for stability, testing of new drug substances and products?
GPAT - 2023
GPAT
Pharmaceutical Jurisprudence
Narcotic Drugs and Psychotropic Substances Act, and Rules thereunder
Match List I and List II
List I: Schedule
List II: Covers the
A
Schedule Y
I
Shelf of drugs
B
Schedule FF
II
Requirements for clinical trials
C
Schedule O
III
Disinfectant liquids
D
Schedule P
IV
Opthalmic ointments
Choose the correct answer from the options given below:
GPAT - 2023
GPAT
Pharmaceutical Jurisprudence
Historical background Drug legislation in India, Code of Ethics for Pharmacists
Requirements of factory premises for the manufacture of cosmetics are mentioned in the Drugs and Cosmetics Rules, 1945 under:
GPAT - 2023
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
Drug covered under this schedule are not permitted for repacking license. Identify the correct schedule.
GPAT - 2023
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
The objective of the Abbreviated New Drug Application is to …
GPAT - 2022
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
As per the Pharmacy Act, in the composition of Pharmacy Council of India, the total number of Ex‐officio members is
GPAT - 2022
GPAT
Pharmaceutical Jurisprudence
The Pharmacy Act 1948
India’s first Central Drug Laboratory was established at
GPAT - 2022
GPAT
Pharmaceutical Jurisprudence
Shops and Establishment Act
Compendium of pharmaceuticals and specialties is an International drug compendia from
GPAT - 2021
GPAT
Pharmaceutical Jurisprudence
Industrial Development and Regulation act 1951
Powers of drug inspectors appointed under the Drugs and Cosmetic Act, 1940 are mentioned under which of the following section of the Act?
GPAT - 2021
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
Match List I with List II
List I
List II
A
Schedule M
I
Regulations regarding Life period and storage of various drugs
B
Schedule FF
II
Regulations for manufacturing, premises, waste disposal, requirements of plant and equipments (Good Manufacturing Practices)
C
Schedule G
III
Various drugs to be used under the medical supervision
D
Schedule P
IV
Standards or Ophthalmic preparations
Choose the correct answer from the options given below:
GPAT - 2021
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
As per the definition of D & C Act, Gudakhu (rubbed against human teeth) is considered as
GPAT - 2020
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
Standards to be complied under D & C act - 1940 for drugs imported, manufactured, stocked and exhibited for sale or distribution are covered under
GPAT - 2020
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
In International organization for standardization (ISO), standard pertaining to quality system model for quality assurance in production, installation and servicing is given under
GPAT - 2020
GPAT
Pharmaceutical Jurisprudence
Standard institutions and regulatory authorities
Who was the Chairman of the Drugs Enquiry Committee which was established in the year 1927?
GPAT - 2020
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
As per the Drugs and Cosmetics Act-1940, if a drug is not labelled in prescribed manner it is a
GPAT - 2020
GPAT
Pharmaceutical Jurisprudence
Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications
Which of the following is not a fundamental (primary) factor considered for selection of a location for the construction of pharmaceutical or chemical plant?
GPAT - 2020
GPAT
Pharmaceutical Jurisprudence
Industrial Development and Regulation act 1951
As per US FDA, NDA’s for new chemical entitles are classified as either :
GPAT - 2019
GPAT
Pharmaceutical Jurisprudence
Standard institutions and regulatory authorities
In India the patent office has its head office at Kolkata and branch offices at :
GPAT - 2019
GPAT
Pharmaceutical Jurisprudence
Intellectual Property Rights and Indian Patent Act 1970
21 CFR part 211 of USFDA describes :
GPAT - 2019
GPAT
Pharmaceutical Jurisprudence
Standard institutions and regulatory authorities
As per the Medical Termination of Pregnancy Act and rules, the safe custody of "Forms" is with:
GPAT - 2019
GPAT
Pharmaceutical Jurisprudence
Medical Termination of Pregnancy Act 1970 and Rules 1975
Prev
1
2
Next