1) តើនៅពេលណាទើបយើងអោយលទ្ធផលជាប់តេស្ត Friability?

2) ក្នុងករណីអ្នកបានធ្វើតេស្ត Disintegration ចំនួន 6 គ្រាប់ មាន១គ្រាប់ធ្លាក់ចេញពី Limit acceptable ។ តើអ្នកសន្និដ្ឋានដូចម្តេច?

3) Which of the following is not correct about High pressure liquid chromatography (HPLC)?

4) The ability of an analytical method to demonstrate how closely the result of an experiment
agrees with the expected result is the definition of?

5) What is Conformance to specification means?

6) The methodology of calibration of glassware are? Choose incorrect answer.

7) 36- Test uniformity of weight, the deviation of individual masses from the average mass more
than 250 mg should not exceed the limits given below?

8) Which one of these is a physicochemical property of Drug substance (raw materials)?

9) នៅពេលធ្វើតេស្ត Disintegration តើអ្នកសង្កេតមើលរបៀបមិច ទើបកត់យកនាទីជាលទ្ធផល?

10) Which one of these is a physicochemical test of Drug substance (Raw materials)?

11) Which form of drug formulation has disintegration time?

12) Which one of these physicochemical tests, is not test of Drug product (finished product)?

13) Définition de la spécification ?

14) The parameters need to be validated for new analytical method development in order to
identification of chemical compounds is?

15) Test Dissolution គឺធ្វើដើម្បី?

16) តើការធ្វើតេស្ត Dissolution ត្រូវអនុវត្តន៍បាននៅសីតុណ្ហភាពប៉ុន្មាន?

17) Which one of these is a microbiological property of Drug product (finished product)?

18) Which one of these physicochemical tests, is not test of Drug substance (Raw materials)?

19) Which one of these is a physicochemical test of Drug product (finished product)?

20) The ability of an analytical method is how well replicate measurements agree with one another,
usually expressed as a standard deviation, express within-laboratories variations: different days,
different analysts, different equipment, etc. is the definition of?

21) In process control (Contrôle en cours de la fabrication) ធ្វើដើម្បី?

22) The calibration based on a calibrated vessel is used as a reference in the calibration of an
unknown vessel, is sometime used when many glassware items are to be calibrated is the
methodology of?

23) Which one of these physicochemical tests, is not test of Drug product (finished product)?

24) Which one of these is a physicochemical test of Drug product (finished product)?

25) Which one of these is a microbiological property of Drug product (finished product)?

26) Why are standard operating procedures important?

27) The requirements of the test disintegration are met if not less than 16 of the 18 dosage units
tested have disintegrated for coated tablet?

28) Which one of these is a physicochemical test of Drug substance (Raw materials)?

29) Which form of drug formulation need to evaluate for dissolution percentage?

30) Analytical method can be divided into two main types?

31) Which one of these physicochemical tests, is not test of Drug product (finished product)?

32) What is QC in pharmaceutical industrials?

33) Which one of these physicochemical tests, is not test of Drug substance (Raw materials)?

34) Which one of these physicochemical tests, is not test of Drug substance (Raw materials)?

35) ក្នុងករណីអ្នកបានធ្វើតេស្ត​ Uniformity of weight ចំនួន២០គ្រាប់ មាន១គ្រាប់ធ្លាក់ចេញពី Limit ទី២។ តើអ្នកសន្និដ្ឋានដួចម្តេច?

36) In the assay of paracetamol tablet, what are the solutions need to run in spectrophotometer?

37) ដើម្បីរកភាគរយនៃភាពសុទ្ធ (Purity) របស់វត្ថុធាតុដើម យើងត្រូវធ្វើតេស្ត?

38) The ability of an analytical method to distinguish analyte from everything else that might be in
the sample is the definition of?

39) Which one of these is a physicochemical test of Drug product (finished product)?

40) តើនៅពេលណាទើបអ្នកអាចសន្និដ្ឋានថាឱសថដែលបានធ្វើតេស្ត ធ្លាក់ Uniformity of weight?

41) ក្នុងករណីអ្នកបានធ្វើតេស្ត​ Disintegration ចំនួន 6 គ្រាប់ មាន៣គ្រាប់ធ្លាក់ចេញពី Limit acceptable។ តើអ្នកសន្និដ្ឋានដូចម្តេច?

42) តើយើងកំណត់ ចំនួននាទីនិងជុំ ទៅលើឧបករណ៍​ Friability tester ដូចម្តេចមុនពេលចាប់ផ្តើមដំណើរការ?

43) La Module 3 du dossier CTD (ou ACTD) est décrit des informations concernent ?

44) Test microbiologique (qualité microbienne) des produits pharmaceutiques est un test qui ?

45) តើយើងត្រូវយកថ្នាំប៉ុន្មានគ្រាប់ទៅធ្វើតេស្ត Friability? សូមបញ្ជាក់

46) Test uniformity of weight, the deviation of individual masses from the average mass less than 80
mg should not exceed the limits given below?

47) We prepare the indicator solution of potassium chromate (K2CrO4, MM = 194.19 g/mol) 5%
(W/V) in 100ml of water, we weight mK2CrO4 ?

48) The range of concentration for analytical method validation is normally set between?

49) The requirements of the test disintegration are met if not less than 16 of the 18 dosage units
tested have disintegrated for uncoated tablet?

50) The ability of an analytical method is the lowest concentration of analyte that can be measured
in the sample matrix at an acceptable level of precision and accuracy, is the definition of?

51) The finished products containing active ingredients should comply with ……………….
composition of the marketing authorization.?

52) Test Disintegration គឺធ្វើដើម្បី?

53) Which one of these physicochemical tests, is not test of Drug substance (Raw materials)?

54) For identification of the unknown sample by spectrophotometry, what is the information we
need from the measurement?

55) ដើម្បីវិភាគរកបរិមាណសារធាតុសកម្មឱសថ (Dossage/Assay) តើមានវិធីសាស្រ្ត (Method) អ្វីខ្លះ?

56) La monographie est ?

57) ក្នុងករណីអ្នកបានធ្វើតេស្ត Uniformity of weight ចំនួន២០គ្រាប់មាន៣គ្រាប់ធ្លាក់ចេញពី Limit ទី១។ តើអ្នកសន្និដ្ឋានដូចម្តេច?

58) Which statement best describes a standard operating procedure (SOP)?

59) The calibration based on the direct mass measurement of water delivered by a pipet or
contained in a volumetric flask and conversion to volume with the density, at the specified
temperature is the methodology of?

60) Which one of these physicochemical tests, is not test of Drug substance (Raw materials)?

61) តើនៅពេលណាទើបអ្នកអាចសន្និដ្ឋានថាឱសថដែលបានធ្វើតេស្ត ជាប់ Uniformity of weight?

62) តើការធ្វើតេស្ត Disintegration ត្រូវអនុវត្តន៍បាននៅសីតុណ្ហភាពប៉ុន្មាន?

63) The ability of an analytical method to obtain test results which are directly proportional to the
concentration (amount) of analyte in the sample is the definition of?

64) The ability of an analytical method is how well replicate measurements agree with one another,
usually expressed as a standard deviation, express under the same operating conditions over a
short interval of time, etc. is the definition of?

65) តើឱសថប្រភេទណាខ្លះតម្រូវឱ្យធ្វើតេស្ត Uniformity of weight? (រកចម្លើយខុស)

66) Les paramètres doivent être écrit dans la monographie sont suivent, excepte ?

67) 35- Test uniformity of weight, the deviation of individual masses from the average mass 80 mg to
250 mg should not exceed the limits given below?

68) The parameters need to be validated for new analytical method development in order to assay of
chemical compounds are included, except?

69) La référentiels de la qualité des matières premières peut trouver dans ?

70) Which one is the correct sequence for drug absorption through the oral route?

71) The ability of an analytical method is the lowest amount of analyte in a sample which can be
detected, is the definition of?

72) The ability of an analytical method is how well replicate measurements agree with one another,
usually expressed as a standard deviation is the definition of?

73) When need calibration of glassware? Choose incorrect answer.

74) The interval between the upper and lower concentration (amounts) of analyte in the sample for
which it has been demonstrated that the analytical procedure has a suitable level of precision,
accuracy and linearity, is the definition of?

75) What is the Concentration in mol/L of 0.1g NaOH , 250ml?

76) Which form of drug formulation has pH in specification?

77) What is the Concentration in C% (W/V) of 4g NaOH, 100ml?

78) តើការកំណត់ Limit acceptable នៅក្នុង Uniformity of weight គេកំណត់ឡើងដូចម្តេចខ្លះ ចំពោះទំរង់ឱសថនីមួយៗ?

79) The parameters need to be validated for new analytical method development in order to testing
for limit of impurities are?

80) Which one of these is a physicochemical property of Drug product (finished product)?

81) In the validation method for assay of paracetamol tablet by spectrophotometer at wavelength
257nm, the solution to be prepared are? Except

82) ក្នុងករណីយើងធ្វើតេស្ត Friability ពេលឧបករណ៍ដំណើរការចប់ មានថ្នាំ១គ្រាប់បែកជា២ តើយើងផ្តល់លទ្ឋផលដូចម្តេច?