Analytical Chemistry Interview Questions
Questions Answers Views Company eMail

inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?

281

Ph meter can show more than 14 ph reading? Why ph range in between 1 to 14 only?

300

How to set specification of assay, fisdolution and related substances?

356

how to qualify the impurity?

316

what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?

334

What is the formula for relative diffrence for standard solution in solution stability in validation?

299

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

706

[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?

300

in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?

341

we can use expired sample for validation and analyst qualification?

292

If vendor having more imp than monograph then how to proceed? and how to set spec?

330

If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately

349

how require to set assay concentration for standard and sample?

359

What is dose dumping? why require to do?

289

Please give idea about method development for cleaning method and how maco level establish

264


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Un-Answered Questions { Analytical Chemistry }

How to know the estimated LOQ concentration in ppm

726


in which situation ion pair require to use?

274


What is column in chromatography?

1755


How doing qbd practically?

419


what is mean by peak intigrity?

334






In Assy by potentio metry titration method how select MET U ,DET U, SET U,

1304


Which are the diffrent grades of api in pharma?

306


How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample

2523


how to qualify the impurity?

316


Is it nessesary all multimedia dissolution require descriminatory?

330


What is Band broading effect explain

1392


Why only 1.2 million lux hours require in photostability study?

454


If vendor having more imp than monograph then how to proceed? and how to set spec?

330


What is stray light in uv what are units for stray light

1012


if content uniformity passing but dissolution varrying then what is next step?

380