What is the basic requirement for preparing drug master file
, like EDMF , USDMF ?
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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 forced degradation study?
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration?
What do you mean by GTT? What are the effect of GTT on film coating.
please explain the job responsibilities of quality assurance..
Job oriented Training in Oracle Clinical, CDM, Clinical Research and SAS with Clinical Trails
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 are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
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.
How to do IR test of hydroscopic materials
Tell us about a time when you failed to meet a deadline. What were the repercussions?
why we have to use only 900 ml buffer in dissolution apparatus ? what are the conditions that favours the selection of volume of buffer?