Answer Posted / mahesh
no unit
| Is This Answer Correct ? | 49 Yes | 14 No |
Post New Answer View All Answers
What is the requirement for brazil in the analytical method vslidation comparr to ich?
Why potassium dichromate is used in calibration of uv?
what is partion and column chromatography
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
how much mass should be there in volumetric flask while in preparation of sample for assay?
is it nessesary to do solution stability for 7 days?
Which parameters require to do in tech transfer?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
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?
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
what is mean by ambient temperature?
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?
Why we use potassium dichromate in uv calibration Exact reason behind it??
WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE