I have got selected for Aurobindo Pharma AR&D, HR person is
asking me to sign in agreement. can I join?
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Answer Posted / pavan
Worst company , heavy work load , waste bosses and waste management , and never get into bonds in any company if u are educated person
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Did anybody have method for acetyl cysteine effervescnce tablet
what is mean by nitrosamine impurities?
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?
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
How we choose the mobile phase for method development.?
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.?
in stress study if your api not soluble in hcl naoh h2o2 then what require to do?
Why perchloric acid used for potentiometric titration
what is classification of elemental impurities? what is risk assement in elemental impurities?
why require to do water content for drug product?
What is a difference between potency and purity?
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.
How can I develope method of dissolution by HPLC OR UV
how to get accurate result for Residue on evaporation in purified water
A ha tc is actual defination of retention time?
