using of chemical standards in HPLC he customer gave 100.2%
what potency i will use this potency in hplc?
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how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis
Why SLS used as dissolution medium
when i come in contact with any metal items or clothes of fur i find myself shock and when run my fingers on fur clothes or matters, i find sparks. Is there any vitiams deffecieny in my body. If so, what i have to do?
Hi Sir?Mam, If i complete SAS CLINICAL in India, can i step forward to USA for job trials? How far is it possible? Am a B.pharm student ,willing to make up my Master's degree too,will this both M.Pharm and SAS help me out to get a job in USA? Please help me out with a good answer.
why nitrogen charecter as a inert gas plz identified
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
Iam a B.PHARMA GRADUATE from DELHI UNIVERSITY and I am looking forward for DRUG INSPECTOR EXAM..kindly mail me any ques papaers reg the same...
How can I assign a retest date for solvents e.g. toluene, methanol, etc?
Tell us about a time when you failed to meet a deadline. What were the repercussions?
What r the different sop in or plant
You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,
WHAT IS MEANING OF DEAIATION WITH EXAMPLE
Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section.
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?