Answer Posted / lingaraj jainar
The amount of drug released in the specified time is called
dissolution.It also finds the bio availability of the drug
in the tablet or capsule
| Is This Answer Correct ? | 18 Yes | 3 No |
Post New Answer View All Answers
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
What is similarity factor?
what is %labelled amount in content uniformity of dosage unit and its calculation?
What is viod volume and peak purity in HPLC?
why are measure gas flow " ml " in Gas chromatography
how to decide for one product require water content or LOD?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
what is the extinction coefficient for Indomethacin or at 319nm wave length.
in OSD forms require to use gas chromatography?
Please give idea about method development for cleaning method and how maco level establish
IS THERE ANY EQUIPMENT TO CHECK AND CALCULATE THE POLARITY OF A LIQUID?
[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?
we can use expired sample for validation and analyst qualification?
what is the procedure for cleaning of lenses of hatr accesory of ftir instrument?
WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE
