Answer Posted / jitendra kumar
dissolution is the drug release specified time in tablet and capsul
Is This Answer Correct ? | 2 Yes | 1 No |
Post New Answer View All Answers
how much mass should be there in volumetric flask while in preparation of sample for assay?
What is the difference between chromatographic purity and related substances?
Why only Copper standard is used to calibrate Atomic Absorption spectrophotometer?
what is definition of validation? which components are followed give detail?
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
How to fix the sample conc. in Related substances test by HPLC?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
calibrtion procedue of LC-MS
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
In Assy by potentio metry titration method how select MET U ,DET U, SET U,
if rsd failed then what require to do?
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
WHAT IS THE CRITERIA FOR SELECTION OF TIME OF DISSOLUTION AND THE MEDIUM OF DISSOLUTION?
in which situation ion pair require to use?