how to start the method development of Dissolution and related
substances.
- 1 Answers
- 11011 Views
- Apex, I also Faced
- E-Mail Answers
Answer Posted / satheesh kumar
Dissolution-Amount of drug release in solid dosage form in
different media.
In dissolution run time should be less,time points are more
(5min,10min,15min,25min,30min and so on)for a single
batch.Primarily check the available impurities not co-elute
with our drug product.
In related substances we are considering about known and
unknown impurities.
| Is This Answer Correct ? | 4 Yes | 6 No |
Post New Answer View All Answers
why we are using benzene, anyline in acetic anhdride assay titration method?
how to calibrate hplc & gc
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
Why only Copper standard is used to calibrate Atomic Absorption spectrophotometer?
why digestion require in icpms?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
What is the formula for relative diffrence for standard solution in solution stability in validation?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
[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?
Tell me something about Vitamin A test method by HPLC
if identification threshold crosses the limits then what next step?
which batch require to use for analytical method validation?
some product having water content method with pyridine and ethylene glycol mixture instead of methanol? how they are selecting and methanol is not suitable solvent how ?
