Pharmacy Interview Questions
Questions Answers Views Company eMail

What do you mean by Q+5 in dissolution?


What is the disintegration time for Hard Gelatin Capsule?

1 4724

What is limit of disintegration for Enteric coated tablets?


5 6461

What should be the sampling point in dissolution test?

1 12286

Which will give more drug release paddle or basket in dissolution?

Aishwarya Healthcare,

2 11487

Tablets of which drug are used in dissolution calibration?

2 8633

What is the difference between Drug Purity and Drug Potency?

1 4846

What should be the minimum limit of a working standard?


What is the storage condition for reference standard?

3 9198

How impurity is analyzed in any tablet?

1 7165

Why we use the placebo in analysis?

2 8334

What is the procedure to prepare the placebo?

4 10367

What is difference between method validation and method verification?

1 2906

What is the technology transfer and how is it done?

2 3816

What are the steps for the sterilization procedure for Dry Powder injection facility (from Starting)?


1 4514

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Un-Answered Questions { Pharmacy }

what are all the parameters to be considered while applying bracketing and matrixing?where and all it is applicable?


Why we said Glacial Acetic Acid to Acetic Acid m


why we study matrixing in stability system in stability study and on what basis we select time point.


how impurity is analyzed in a tablet


What is the calibration of HPLC?


How to conduct Literature Survey for Generics Development for European Market


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.


Can you please mail me the latest syllabus of UTTAR PRADESH DRUG INSPECTOR entrance exam and UTTAR PRADESH FOOD INSPECTOR entrance exam with the eligibility criteria for Uttar Pradesh domicile candidates.


How to check the integrity of Sieve, Screen, FBD Bag?


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


what is limit of cleaning validation


why we use matrixing method in stability study and on what basis time points are selected?


why u want to join as a m.r?


what we do when calibration of any instrument is fail ?


when will be the drug inspector notification will be anounced.what are the educational requirements...