How to determine peak purity index in Empower software? What is the acceptance criteria of peak purity index to consider the peak purity is pass?591
What is medical representative role ?1 493
how to make Enrofloxacin 20% solution & whats remedy to avoid crystal formation in this batch after 15 -20days? Please anybody assist in it487
what is difference between usfda and mhra guidline417
In resolution test of uv calibration ratio of 269nm & 266nm, respectively, using hexane as the reference . the acceptance criteria for the ratio is NLT 1.5 but always found that 1.3 ,why what i can do for the resolving the problem is it necessary to integrate exat at 269nm and 266nm ehat is limit of tollerence179
What is the Disintegration time for Hard gelatin Capsule in USP?186
i am little a bit confused on, who was the father of pharmacy either galen or william procter. please someone clarify this to me1 211
besides Signal & noise ratio how calculating LOD & LOQ?
What do you mean by Bracketing and Matrixing in stability?
What is the difference between Analytical method validation and Analytical method transfer?
why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc
In resolution test of uv calibration ratio of 269nm & 266nm, respectively, using hexane as the reference . the acceptance criteria for the ratio is NLT 1.5 but always found that 1.3 ,why what i can do for the resolving the problem is it necessary to integrate exat at 269nm and 266nm ehat is limit of tollerence
i had completed my degree with 72% but i dont have good score in gre and tofel and i got an admission into a college in usa is trheir will be any problem if i appear for visa regection because of gre and tofel and i am from science background i lost touch in those subjects.
how related substnce method developted for new compound which not official in the pharmacopiea
When we change water of Hygrometer?
Why we use pyrene in HPLC calibration ( UV-vis/PDA)
If granules are over lubricated what defect arises in tablet compression how we solve this problem.
how impurity is analyzed in a tablet
In Stability testing if significant change occurs then what will be the action plan?
principle of dissolution
i am from orissa .can you please send me the question papers of drug inspector exam of orissa ?my email id is email@example.com've completed my b.pharma can i apply for d.i exam ?
how you can fix the known and unknown impurity limit for any drug substance