Interested to Buy Any Domain ? << Click Here >> for more details...
what is the use of tap density apparatus? why we calculate
it? what is the difference between the bulk density and tap
density?
- 1 Answers
- 5237 Views
- Alchemist, Alembic, Apex, I also Faced
- E-Mail Answers
Answer Posted / asm
It is tested to know the flow properties of the powder.this study is known as Rheology.practically,in the production when the powder is filled into the Hooper or some other it has to move and fill into a vial or should be punched to get a tablet.this tapped density value indicates whether the powder is free flowing or sticky like that.for such reasons we calculate tapped density.and we will have a specification limit etc.
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
what is the origin to prepare standard operating procedure
which batch require to use for analytical method validation?
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
on the basis of bcs class how to proceed the solubility?
We use hicrome 10 cxs column in hplc analysis....pls tell me.. what is the meaning of 10 cxs?
why require to do water content for drug product?
what are the guidelines for analytical method validations?
if instrument calibration fails then what require to do?
what is mean by peak intigrity?
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
How to know the estimated LOQ concentration in ppm
how the compound separate in coulunm,explain
As per ICH related substances stability trend limit from initial to shelf life
How we can identify process related and degradation impurity in single method with short period?
