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.
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
WHAT IS MEANING OF DEAIATION WITH EXAMPLE
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?
what is the mechanism of action of local anaesthetics?
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that
please explain the job responsibilities of quality assurance..
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.
from hplc chromatogram how can we say that calibration is needed now?
difference between RF and correction factor?
what is the leak test procedure of filled bottles (liquid)
What r the different sop in or plant
why nitrogen charecter as a inert gas plz identified