Pharmacy Interview Questions
Questions Answers Views Company eMail

How we fix the validity period of a volumetric solution and re-standardization due date?


How quantitative stability studies are done?

Reddy Labs,

1 3865

What do you mean by CAPA?

2 5543

In KF Standardization why we use Disodium Tartarate?

1 4437

What is the difference between Deviation and Out of Specification?



What is the difference between mix-up and cross-contamination?


What is GMP, cGMP and GLP?

1 9581

What is the calibration of HPLC?


How polarimeter is calibrated?

1 872

What is the difference between Analytical method validation and Analytical method transfer?


How melting point apparatus is calibrated?

1 4280

What is the difference between polarimeter lamp and IR lamp?


What is the difference between sonication and homozinization?


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


What is limit of uniformity of content as per USP?

3 2807

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Un-Answered Questions { Pharmacy }

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


Why we use potassium hydrogen pthalate for determination of calibration in Total organic carbon


Hai,i had completed my want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at


is there any entrance exam conducted for the post of drug inspector and what is the usual time


How to select temperature of ODT in disintegration test


What should be Step wise the sterlization procedure for Dry Powder injection facility (from Starting)?


what is recovery factor


how related substnce method developted for new compound which not official in the pharmacopiea


if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?


How related substance method is developed for new compound which is not official in the pharmacopeia?


hello friends... i got 3 tym rejection in my us student visa interview. every tym vo ask me same questions lyk y ths uni, y ths course n abt my sponsor etc. pls gv me suggestion for th que, y ths uni? as my undergraduate major is pharmacy n i got i 20 frm university of bridgeport for ms in biomedical eng.


what is purpose of slow,medium,fast sampling in process validation ?


What do you mean by Q+5 in dissolution?


What is the difference between mix-up and cross-contamination?


i had completed my degree with 72% but i dont have good score in gre and tofel and i got an admission into a college in usa is trheir will be any problem if i appear for visa regection because of gre and tofel and i am from science background i lost touch in those subjects.