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Health Pharma AllOther Interview Questions
Questions Answers Views Company eMail

Which types of deviations are followed in pharmaceuial API manufacturing industry?

Laurus,

1 4471

What are the significance of MKT in stability study.

Alembic,

1 7462

What is the different between GMP & cGMP ?

1 7580

what is the mechanism of action of local anaesthetics?

2283

why we have to use only 900 ml buffer in dissolution apparatus ? what are the conditions that favours the selection of volume of buffer?

1 7181

what is the disintegration time of mouth dissolving tablet

Unimarck Pharma,

3 7850

How to register or submit drug master file to any regulatory agency?

2 7021

while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that

2602

please explain the job responsibilities of quality assurance..

2379

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.

Alchem, Getz Pharma Research, Hovid Berhad,

2711

How to set impurity limits for Related substances test.

1 4706

using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc?

Vivimed Labs,

1 3495

Tolerance limit for dissolution media rpm sampling point.

Torrent Pharma,

1 3958

diffrence between known impurity and specified impurity?

Cipla, Medreich,

2 7048

from hplc chromatogram how can we say that calibration is needed now?

Lupin, Teva Pharmaceuticals,

2547


Post New Health Pharma AllOther Questions

Un-Answered Questions { Health Pharma AllOther }

What aspect of your communications skills have you improved the most in and how did you accomplish this improvement?

2381


plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,

2439


when we connect the capacitor banks in series with the circuit? 2 144 pH is having unit?

2258


What experience do you have in training?

2456


What r the different sop in or plant

1979


how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis

9020


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...

2203


how many clauses are there in iso? give me the clauses details?

2672


What is difference between Warm and Lukewarm Water as per pharmacopia.

1529


How should the Medical Librarian interact with training staff?

2278


How are you qualified for the position of Assistant Clinical Director?

2502


why you are become a medical representative

2184


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.

2169


please explain the job responsibilities of quality assurance..

2379


What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan

2361