Analytical Chemistry Interview Questions
Questions Answers Views Company eMail

what is classification of elemental impurities? what is risk assement in elemental impurities?

408

what are risk assement in the analytical qbd?

342

why multimedia dissolution require to do?

371

in OSD forms require to use gas chromatography?

399

why require to do water content for drug product?

390

before starting analytical method valodation what you checking? and how giving preference to start validation?

430

in which situation ion pair agent require to use?

330

effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?

409

if you given one product then which tests you will perform?

371

on the basis of bcs class how to proceed the solubility?

347

for which product require to do content uniformity? what is limit of cu?

396

how require to select dissolution media? what is discrimination?

388

if rsd failed then what require to do?

400

if peak get problamatic then what require to do?

392

how you confirm the assay method?

349


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Un-Answered Questions { Analytical Chemistry }

[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?

431


In Dissolution Test why limit is define Q+5% what is the role of +5%.

2644


How to fix the sample conc. in Related substances test by HPLC?

689


How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.

1852


How to establish relative response factor for hplc. Why it is required?

792






What is shaking level in GC?

395


in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?

407


how to develop the icp ms method? Application of icp ms?

407


How to know the estimated LOQ concentration in ppm

800


How require to perform linearity as per ANVISA? What are the acceptance criteria?

816


how can give the expiry period and restadardisation of volumetric solution

2137


Which parameters require to do in tech transfer?

344


Why dissolution test is not performed in all of the products

2113


iam usig ph buffers merk. manually how to prepare ?

1840


As per ICH related substances stability trend limit from initial to shelf life

2768