define the starting material?
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What is the difference between mix-up and cross-contamination?
What will be in case stability sampleWhich have batch but distribute in three country.In tath case< we can put the sample for all country, whenevr all have same temp(Zone)
How would you manage your team for pahrmaceutical representatives?
Why and When RRF is necessary in RS method? How it is helpful in method development?
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what happen if diameter of colum increse in gas chromatography?
basic of hplc,columns used
What is the difference between Drug Purity and Drug Potency?
What is validation, validation protocol and validation master plan?
Hai,i had completed my M.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 vislawath.jyothi@gmail.com
how will convience the doctor
Why do you want to make a career in pharmaceutical?
what we do when calibration of any instrument is fail ?