Answer Posted / t reddy
quality control is a set of procedures to check whether the drug products is achieving the customers needs or not.....
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
What is a difference between potency and purity?
Loss of linearity in tkn analysis, possible reasons?
how to develop the icp ms method? Application of icp ms?
pharma industries oriented
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
how you fix the limits of impurities?
What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
From where require to take the RLD sample?
Describe your field experience sample type collected,sample techniques,field measurements taken and equipment used?
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
Why are use silicon oil mr?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?