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Assume that you've been hired for the position. A mother calls and says her child is sick and she needs an appointment this morning. You don't have an open appointment for the morning. What will you do?
1 4409You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.
2145what is the diffirence between deviation and change control? at what situations we can raise the deviation and change control
Biocon, Cipla, DRL, Glenmark, Granules, Lupin, Micro Labs, Mylan, Natco, Ranbaxy, Swissmedic,
31 169284IF We have to autoclave two chamber of media one having temp 100 c and onather at RT,which one get autoclaved first?
1 5376Iam 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...
2206Post New Health Pharma AllOther Questions
what is the mechanism of action of local anaesthetics?
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
How to perform forced degradation on tablet sample or suspensions?
How should the Medical Librarian interact with training staff?
How to preform dissolution profiling
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
What is the role of buffers (ex: KH2PO4) in HPLC analysis,
what is ur strengths and weekness in ur professional life as medical rep?
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.
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.
How to do IR test of hydroscopic materials
please e-mail me the model of Tamil Nadu drug inspector question papers
What is difference between Warm and Lukewarm Water as per pharmacopia.
