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
What are the regulatory commitments in markets like USA,
Canada, Europe, Brazil, South Africa and Japan
What are your intentions towards the uplift of the hospital.
while formulation of Gliclazide floating tablets why we are
using direct cmpression technique why not wet granulation and
what happend with that
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.
Tolerance limit for dissolution media rpm sampling point.
why an employee go for medical representative instead of quality?
what is the
action of local
plz.mail me model papers of drug inspector of chhattisgarh..or
MP.if Posible. Mail
What skills have you acquired that would apply to the
position of Clinical Data Manager?
What experience do you have in training?
what is your experience in medical continuing education.
How are you qualified for the position of Assistant
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...
what is meant by artwork review and handling procedure with
What is the basic requirement for preparing drug master file
, like EDMF , USDMF ?