what is stationary phase4 7509
what is difference between vacuum pressure and vapor pressure1 25580
there are how many leak sensor in shimandzu hplc,agilent hplc,dionex hplc and water's hplc?3 5890
Why Naphalene only used in calibration of HPLC2 3748
In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?1 3563
In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?1605
what happen if diameter of colum increse in gas chromatography?2 4201
Whhat is the justification for stability study in api missed stations through deviations and statistical analysis is required.
if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?
hi i have done my b pharma and now i am working as a managing director in my own manufacturing unit is there any scope overthere 4 me
hai,i had completed my b.pharmacy.i want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at email@example.com
when will be the drug inspector notification will be anounced.what are the educational requirements...
i am preparing for Drug inspector exam.If u have previous questions please send me.
HI, I srinivas , was shortlisted for interview of Ph.D. PROGRAMMES FOR ACADEMIC SESSION 2012, I have interview on 17-nov-2011. Sir can you tell me about interview, how to prepare for it. How it will be? It's my first interview sir, i don't know how to face it. Kindly help me sir, Thanking yoU,
What is the relative response factor in related substances?
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
what are the most common infectious diseases a pharmacist sees? Do pharmacists routinly encounter antibiotic resistent in some of the infectious agents that patients have contacted? if so which onces?
What is limit of cleaning validation?
how to select HPLC column for a particular product
if calibration of 12 bowl dissolution apparatus does not meet a single stage procedure how you can proceed calibration
principle of dissolution
How related substance method is developed for new compound which is not official in the pharmacopeia?