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

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

3) Test Dissolution គឺធ្វើដើម្បី?

4) ដើម្បីរកភាគរយនៃភាពសុទ្ធ (Purity) របស់វត្ថុធាតុដើម យើងត្រូវធ្វើតេស្ត?

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

6) តើឱសថប្រភេទណាខ្លះតម្រូវឱ្យធ្វើតេស្ត Uniformity of weight? (រកចម្លើយខុស)

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

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

9) 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?

10) តើការធ្វើតេស្ត Disintegration ត្រូវអនុវត្តន៍បាននៅសីតុណ្ហភាពប៉ុន្មាន?

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

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

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

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

15) 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?

16) តើយើងកំណត់ ចំនួននាទីនិងជុំ ទៅលើឧបករណ៍​ Friability tester ដូចម្តេចមុនពេលចាប់ផ្តើមដំណើរការ?

17) 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?

18) What is QC in pharmaceutical industrials?

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

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

21) Which form of drug formulation has disintegration time?

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

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

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

25) 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?

26) 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?

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

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

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

30) តើនៅពេលណាទើបយើងអោយលទ្ធផលជាប់តេស្ត Friability?

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

32) 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?

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

34) Définition de la spécification ?

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

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

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

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

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

40) តើយើងត្រូវយកថ្នាំប៉ុន្មានគ្រាប់ទៅធ្វើតេស្ត Friability? សូមបញ្ជាក់

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

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

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

44) តើការធ្វើតេស្ត Dissolution ត្រូវអនុវត្តន៍បាននៅសីតុណ្ហភាពប៉ុន្មាន?

45) 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?

46) នៅពេលធ្វើតេស្ត Disintegration តើអ្នកសង្កេតមើលរបៀបមិច ទើបកត់យកនាទីជាលទ្ធផល?

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

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

49) La monographie est ?

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

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

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

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

54) 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?

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

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

57) What is Conformance to specification means?

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

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

60) 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?

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

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

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

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

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

66) តើនៅពេលណាទើបអ្នកអាចសន្និដ្ឋានថាឱសថដែលបានធ្វើតេស្ត ធ្លាក់ Uniformity of weight?

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

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

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

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

71) 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?

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

73) Why are standard operating procedures important?

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

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

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

77) Test Disintegration គឺធ្វើដើម្បី?

78) តើនៅពេលណាទើបអ្នកអាចសន្និដ្ឋានថាឱសថដែលបានធ្វើតេស្ត ជាប់ Uniformity of weight?

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

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

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

82) ក្នុងករណីយើងធ្វើតេស្ត Friability ពេលឧបករណ៍ដំណើរការចប់ មានថ្នាំ១គ្រាប់បែកជា២ តើយើងផ្តល់លទ្ឋផលដូចម្តេច?