Pharmacy Interview Questions
Questions Answers Views Company eMail

what do you mean by mean kinetic temperature in stability

2 13247

what do you mean by bracketing and matrixing in stability

1 3894

how to select HPLC column for a particular product

2674




what is the composition of C18 column

Cipla, Deccan,

2 22455

what is limit of cleaning validation

1242

what is recovery factor

Jubilant,

1054

how much the minimum recovery should be in swab sampling

1 9902

what do you mean by Q+5 in dissolution

1 20299




what is difference between in drug purity and drug potency

2 2736

what should be minimum limit of working standard

1 14072

how impurity is analyzed in a tablet

2021

what is difference between method validation and method verification

1 1697

what should be the LOD of dry syrup

1 4866

how you can fix the known and unknown impurity limit for any drug substance

1841

what is relative response factor in related substance

2 4143


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Un-Answered Questions { Pharmacy }

why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc

1722


Delay in receiving offer letter? Dear All, Recently I clear all technical and HR round with one good MNC. I've submitted my scan document of qualification and work experience. Evenafter 2 weeks of sending documents, they didn't release the offer letter. Please suggest me effective email contents to deal them. Thank You

1943


at what interval Ukrainian audit will come once you register your product??

992


when we calibrate uv for control of wavelength we scan for 200 to 800 nm but we get the result only for some specific wavelength how we confirm for all other wavelength?

1210


What is the difference between uniformity of content and content uniformity as official test for all tablets?

1412






What is main of k*abs in uv visible spectroscopy

963


what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)

636


what are the most common infectious diseases a pharmacist sees? Do pharmacists routinly encounter antibiotic resistent in some of the infectious agents that patients have contacted? if so which onces?

1210


what is limit of cleaning validation

1242


i am preparing for Drug inspector exam.If u have previous questions please send me.

1607


what is difference between usfda and mhra guidline

872


HOW TO PERFORM SATURATION SOLUBILITY IN DISSOLUTION METHOD DEVELOPMENT?

2525


the international interview procedure for a job.

1127


In resolution test of uv calibration ratio of 269nm & 266nm, respectively, using hexane as the reference . the acceptance criteria for the ratio is NLT 1.5 but always found that 1.3 ,why what i can do for the resolving the problem is it necessary to integrate exat at 269nm and 266nm ehat is limit of tollerence

315


What is validation, validation protocol and validation master plan?

1237