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How will you calculate telling in any HPLC peak?
What is limit of cleaning validation?
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
How we fix the validity period of a volumetric solution and re-standardization due date?
Why we use disodium tartare for determination of factor in karl ficher titration?
Dear friens,this is sreedhar i am a pharmacy post graduate and having 3 years of experience in pharma industry. I am searching job in USA. through that i want to apply H1,please sugeest me how can i search job or is there any consultancies in india help me to get job?
What is limit of uniformity of content as per USP?
what is the defintion of Pka?
Why 3X sampling plan are implemented in process validation?
what is validation , validation protocol and validation master plan?
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?
define the starting material?