Interested to Buy Any Domain ? << Click Here >> for more details...
What are the limits for uniformity dosage content for tablets and capsules
- 5 Answers
- 23117 Views
- Micro Labs, I also Faced
- E-Mail Answers
Answer Posted / robi
Acceptance value for 10 tablets is less than 15%
| Is This Answer Correct ? | 22 Yes | 1 No |
Post New Answer View All Answers
If combination product how require to identify which imp is of which api?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
in each media we require to use SLS? how to proceed?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
What is a difference between potency and purity?
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
what is mean by covalidation
in gas chromatography what is the difference between gas flow rate and average linear velocity ?
is it nessesary to do solution stability for 7 days?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
how require to select dissolution media? what is discrimination?
how the compound separate in coulunm,explain
what is procedure of actual procedure for registration of drug?
process of Diclofenac sodium,IP.
