2marks, 31 to 35,Jurisprudence Quiz

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Muthukrishnan

India

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2marks, 31 to 35,Jurisprudence Quiz


2marks, 31 to 35,Jurisprudence QuizVersión en línea Finish this Quiz and post the screenshot in this group por Muthukrishnan 1 Primary objective For Pharmaceutical legislation Formulation in india Choose one or more answers a Protect the consumer from Substandard medicine b Protect the consumer from dangerous medicine c Protect the consumer From over pricing d Protect the consumer from Disease 2 Which book having the drugs syandards of strength, quality, and purity ? a BP b USP c IP d USSRP 3 Main objectives of Pharmaceutical Legislation regarding Formulation a Ensure standard Quality b Regulate the import of Formulation c Prevent the animals from killing d Prevent the manufacture of Spurious or adulterated Formulations 4 Schedule C Choose one or more answers a Oral tablets b Insulin c Vaccines d Sera and Toxins 5 SCHEDULE C Choose one or more answers a Orals and antibiotics b Other special products c Biological and special products d Injectables 6 A license For schedule C products is granted in a Form 48 b Form 10 c Form 28 d Form 72 7 Most of the schedule C drugs are stored under a Room temperature b 2 to 8 ° C c 10 to 15 ° C d 15 to 25 °C 8 SCHEDULE C1 a Injectable b Other special products c Ergot and Digitalis d Fish liver oil e Non injectable antibiotics 9 Right to information Act a 2005 b 1985 c 1965 d 1955 10 In the Pharmaceutical Sector, The RTI act allows to know the information From the bodies like a Commercial Tax department b Revenue Department c PCI d The central Drugs Standard control Organization (CDSCO) e Government Hospitals and Universities 11 In RTI The information should be provide with in _____ days to the request person a 30 days b 45 days c 15 days d 7 days 12 EXEMPTION Fron RTI (the information will not be provided from the RTI ) a State pharmacy councils b Integrity of india c Trade secrets d Intellectual property 13 Who is RMP (REGISTER MEDICAL PRACTITIONER) a A pharmacist b A Doctor c A health care professional d A Medical Officer 14 Indian medical degrees act and Indian medical Council Act a 1956 and 1916 b 1940 and 1948 c 1916 and 1956 d 1948 and 1940 15 The Document or a set of Documents that serves as the Blue print For the production of Specific Drug Product is called ? a IP b CIMS c Master Formula record d Medical Dictionary 16 Master Formula record contains a Name, Dosage Form and Strength of the product b A complete list of active ingredients and excipients c The expected amount of the finished product d Step by step instructions e Specifications of the machinery to be used f Storage and labelling

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2marks, 31 to 35,Jurisprudence Quiz

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2marks, 31 to 35,Jurisprudence QuizVersión en línea

por Muthukrishnan

Primary objective For Pharmaceutical legislation Formulation in india

Choose one or more answers

Which book having the drugs syandards of strength, quality, and purity ?

Main objectives of Pharmaceutical Legislation regarding Formulation

Schedule C

Choose one or more answers

SCHEDULE C

Choose one or more answers

A license For schedule C products is granted in

Most of the schedule C drugs are stored under

SCHEDULE C1

Right to information Act

In the Pharmaceutical Sector, The RTI act allows to know the information From the bodies like

In RTI The information should be provide with in _____ days to the request person

EXEMPTION Fron RTI (the information will not be provided from the RTI )

Who is RMP (REGISTER MEDICAL PRACTITIONER)

Indian medical degrees act and Indian medical Council Act

The Document or a set of Documents that serves as the Blue print For the production of Specific Drug Product is called ?

Master Formula record contains