Describe your experience with quality assurance and quality
control analyses?
Answer Posted / mm afsal
QC- is ensure the total quality of of the Drugs in
differnet stages (Raw,Intermediate and FG)using very
stringent policys and meet the product for international
regulatory needs. QC is the significant Department under QA.
QA- is working for the total quality of the manufacturing
process and enusring that all the system which is requiered
for cGMP. QA have right to amend or impliment changes in
the system.Cosider one drawing: we are using may colours,
colours are the deparments in a system and we are using
brush for sketch the idea. If the brush is damaged the
total picture is become bad.
Is This Answer Correct ? | 8 Yes | 0 No |
Post New Answer View All Answers
process of Diclofenac sodium,IP.
How to set analyticl specification for combination products?
how require to interprit the method precision data of hptlc?
How to fix the sample conc. in Related substances test by HPLC?
How to establish relative response factor for hplc. Why it is required?
how you determine moist.of NaOH sol or NaOH flacks
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
Describe your field experience sample type collected,sample techniques,field measurements taken and equipment used?
why multimedia dissolution require to do?
why cone formation during dissolution?
Is it nessesary all multimedia dissolution require descriminatory?
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
what you do when compound having dwel wavelength?
in which situation require to change rs specification?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development