I have got selected for Aurobindo Pharma AR&D, HR person is
asking me to sign in agreement. can I join?
Answer Posted / bhargav kp
Recently I have joined in aurobindo pharma u16 ,jadcherla as a process engineer, they are using b.tech graduates as machine operators by giving them minimum wages , they don't give leaves they torture you for work and the department heads are not worth their roles , please avoid this company and be safe
Is This Answer Correct ? | 6 Yes | 0 No |
Post New Answer View All Answers
if content uniformity passing but dissolution varrying then what is next step?
pharma industries oriented
in api coa contains only process impurities and in product coa contains degradation impurities?
in OSD forms require to use gas chromatography?
If combination product how require to identify which imp is of which api?
How we can identify process related and degradation impurity in single method with short period?
Which type of column should i use to check the purity of high molecular weight protein using HPLC reverse phase column chromatography? Hi everyone. I wanna to check the purity of high molecular weight protein (collagen) with MW of ~130 kDa using a HPLC. I know C18
In HPLC calibration, caffeine is used as primary standard for wave length calibration due to caffeine is having dual maxima at 273 & 205 nm and one minima at 245 nm. Any body can give reference of these details from any pharmacopeia (with chapter no.) or any other authentic guideline?
Which parameter require to do for analytical method equivalency?
sop of a uv visible spectrophotometer double beam elico model
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?
if identification threshold crosses the limits then what next step?
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
analytical method validation require to with respect to release specification or shelf life specification?