尚廷痰九噶乾某市趁列翁匹退
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起止时间:2021-03-15到2021-06-30
更新状态:每5天更新一次
1.Drug Quality Standard and Quality Control Quizzes：Drug Quality Standard and Quality Control
1、 The principle of English names for drugs in Chinese Pharmacopoeia follows（ ） formulated by the World Health Organization.
A:ChP
B:CADN
C:INN
D:BNF
答案: INN
2、 The content of pharmaceutical preparations is expressed as （ ）.
A:Weight percentage
B:Molar percentage content
C:Volume percentage
D:Labeled amount percentage content
答案: Labeled amount percentage content
3、 According to the provisions of drug quality standards, evaluating the quality of a drug uses （ ）.
A:Identification, inspection, quality determination
B:Bioavailability
C:Physical properties
D:Pharmacological effects
答案: Identification, inspection, quality determination
4、 The full name for ICH is （ ）
A:Import drug registration standards
B:European Pharmacopoeia
C:United States Pharmacopoeia-National Formulary
D:International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use
答案: International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use
5、 In Chinese Pharmacopoeia, the general analysis and determination methods are contained in（ ）
A:Volume I
B:Volume II
C:Volume III
D:Volume IV
E:Supplement
答案: Volume IV
6、 Regarding the Chinese Pharmacopoeia, the most appropriate statement is （ ）
A:A book about drug analysis
B:A book containing all medicines produced in China
C:National legal technical standards for supervision and management of drug quality
D:A dictionary about drugs
E:Technical specifications on Chinese herbal medicines and Chinese patent medicines
答案: National legal technical standards for supervision and management of drug quality
7、 There are a total of 36 pieces raw materials entering a factory, and the number of random samples should be （ ）
A:5 pieces
B:6 pieces
C:7 pieces
D:36 pieces
答案: 7 pieces
8、 The basic sequence of drug inspection work is （ ）
A:retain samples → inspection → sampling → report
B:inspection → sampling → retaining sample → report
C:sampling → inspection → report → sample retention
D:sampling → inspection → sample retention → report
答案: sampling → inspection → sample retention → report
9、 ”Precision weighing” in “Chinese Pharmacopoeia” means that the weight should be accurate to （ ） of the weight taken.
A:± 10%
B:1%
C:1‰
D:1‱
E:millionth
答案: 1‰
10、 ”Easily soluble” means that 1g (ml) of solute can be dissolved in ( ) solvent.
A:Less than 1ml
B:1ml～10ml
C:10ml～30ml
D:100ml～1000ml
E:1000 ml～10000ml
答案: 1ml～10ml
11、 The cool and dark place of the drug storage conditions means （ ）
A:No more than 20 ℃
B:Avoid light, not exceeding 20 ℃
C:2 ℃ ～ 10 ℃
D:Avoid light, 10 ℃ ～ 30 ℃
E:Avoid light, 10 ℃ ～ 25 ℃
答案: Avoid light, not exceeding 20 ℃
12、 The requirements for drug inspection sampling are （ ）
A:Scientificalness
B:Authenticity
C:representativeness
D:rigorism
答案: Authenticity;
representativeness
13、 The drug quality standard is （ ）
A:Technical regulations on drug quality specifications and inspection methods
B:Legal basis followed by departments engaged in pharmaceutical production and inspection
C:The legal basis followed by the drug supply and use departments
D:Legal basis followed by drug supervision and administration departments at all levels
E:Contents that must be included in the drug instructions
答案: Technical regulations on drug quality specifications and inspection methods;
Legal basis followed by departments engaged in pharmaceutical production and inspection;
The legal basis followed by the drug supply and use departments;
Legal basis followed by drug supervision and administration departments at all levels
14、 In the following methods, ( ) can be used to identify drugs.
A:Chemical methods
B:Spectrophotometry
C:Chromatography
D:Biological methods
E:Nonaqueous titration
答案: Chemical methods;
Spectrophotometry;
Chromatography;
Biological methods
15、 The content contained in Volume IV of the Chinese Pharmacopoeia 2015 edition includes（ ）
A:Chinese herbal medicines and prescriptions
B:Standards for chemical medicines
C:General notices and general chapters
D:Standards for biological products
E:Standards for medicinal excipients
答案: General notices and general chapters;
Standards for medicinal excipients
2.Pharmaceutical Analysis Methodology Quizzes：Pharmaceutical Analysis Methodology
1、 Using chemical analysis and instrumental analysis to determine drug content is referred to as ( ) in drug quality standards.
A:potency determination
B:biological standardization
C:content determination
D:drug control
答案: content determination
2、 The determination of drug content by biological or enzymatic chemical methods is called ( ).
A:potency determination
B:bbiological standardization
C:content determination
D:drug control
答案: potency determination
3、 Titrate is ( ) for each 1 ml of titrant at the specified concentration.
A:the mole number of the drug measured
B:the mass of the drug measured
C:the mole number of the standard substance
D:the mass of the standard substance
答案: the mass of the drug measured
4、 In the following statements of volumetric analysis used for content determination, the incorrect one is ( ).
A:simple operation
B:accurate results
C:good durability
D:high specificity
答案: high specificity
5、 According to pharmacopoeia, the precisely calibrated titrant (such as hydrochloric acid and its concentration) is correctly expressed as ( )
A:Hydrochloric acid titrant（0.1520M）
B:Hydrochloric acid titrant（0.1520mol/L）
C:Hydrochloric acid titrant（0.1520M/L）
D:0.1520M Hydrochloric acid titrant
答案: Hydrochloric acid titrant（0.1520mol/L）
6、 In volumetric analysis, the burette reading can be estimated to be ±0.02ml. In order to ensure the error of analysis results not exceed 0.1%, the volume of titrant should be ( ).
A:10ml
B:15~20ml
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