Interested to Buy Any Domain ? << Click Here >> for more details...
What is limit of uniformity of content as per USP?
- 3 Answers
- 6926 Views
- I also Faced
- E-Mail Answers
Answers were Sorted based on User's Feedback
If we get 100% assay of an Initial sample ,and the stability studies of the same sample got 90% dissolution result, and when the same stability sample was analyzed for RS studies no impurities was found . Where the 10% Active substance were gone during dissolution analysis.Please help me in getting the conclusion.
why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc
the international interview procedure for a job.
what is difference between usfda and mhra guidline
What are closely monitor parameters in stability study?
i have completed b. pharmacy .i want model papers for drug inspector examination
Difference Between Purity And Potency?
3 Answers Dr Reddys, Reddy Labs, Watson Pharmaceuticals,
how quantitative stability studies are done?
Why we are using propyl parabben in methanol in calibration of hplc for GPV test??
If a drug possesses zwitter ionic nature then can it plays any important role in pharmacy?
3 Answers Cipla, Orion Laboratories,
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
How to select temperature of ODT in disintegration test
Pharmacy 
