What are the limits for uniformity dosage content for tablets and capsules
Answer Posted / vivek pradhan
20
| Is This Answer Correct ? | 1 Yes | 11 No |
Post New Answer View All Answers
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
why are measure gas flow " ml " in Gas chromatography
How to set specification of assay, fisdolution and related substances?
what is mean by 40 in the dissolution basket mesh size?
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
Qc interview questions
How to set analyticl specification for combination products?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
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 the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
Why we check moisture,ash & AIA in product
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
How to establish relative response factor for hplc. Why it is required?