How to define samples weight in moisture content
According to USP general chapter<921>where the specimen under test is capsule,use a portion of mixed contents of not fewer than 4 capsules.when specimen under test is tablets,use powder from not fewer than 4tablets ground to fine powder in an atmosphere of temperature and RH known not to influence the results.
Thanks,
B.Gangatharan,
Caplin point,
Pondicherry.
| Is This Answer Correct ? | 2 Yes | 0 No |
what is difference between drug products and drug substance?
what is mean by 40 in the dissolution basket mesh size?
1)why use benzophenon,uracil in hplc calibration. 2)why use sucrose in polarimeter calibration. 3)what is S/N ratio, noise and drift in hplc 4)how we can find lod and loq in method validation
Defination of ZEEMAN EFFECT in NMR ?
Why pH range is 1-14 nt more than 14???
3 Answers IPCA, Lincoln Pharmaceuticals,
What id the resolution factor
what is the meaning of PURITY AND POTENCY .what is the difference between PURITY and POTENCY
Why do we use 500ppb sucrose and 500ppb 1,4 benzoquinone in TOC calibration?
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 v define from IR & NMR spectroscopy ?
Why base line not start from zero in GC Chromatography analysis.
Why forced degradation studies are performed in hplc method validation?