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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 3521

What are the significance of MKT in stability study.

Alembic,

1 6572

What is the different between GMP & cGMP ?

 1 6830

what is the mechanism of action of local anaesthetics?

 1783

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 6348

what is the disintegration time of mouth dissolving tablet

Unimarck Pharma,

3 6519

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

 2 6048

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

 2088

please explain the job responsibilities of quality assurance..

 1873

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,

2250

How to set impurity limits for Related substances test.

 1 4024

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

Vivimed Labs,

1 2829

Tolerance limit for dissolution media rpm sampling point.

Torrent Pharma,

1 3137

diffrence between known impurity and specified impurity?

Cipla, Medreich,

2 5928

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

Lupin, Teva Pharmaceuticals,

2113

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Un-Answered Questions { Health Pharma AllOther }

why you are become a medical representative

1691

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

8230

Tell us about a time when you failed to meet a deadline. What were the repercussions?

2053

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.

1692

what is the mechanism of action of local anaesthetics?

1783




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

1058

please e-mail me the model of Tamil Nadu drug inspector question papers

2201

Do you think it is possible to rehabilitate?

1733

what is factor?

1758

What skills have you acquired that would apply to the position of Clinical Data Manager?

2060

what is meant by artwork review and handling procedure with an example?

1615

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

1937

pls send me last two years solved papers of health & malaria inspector to kumar.santosh087@yahoo.com

1562

Tell us about a situation in which you took the extra step for a patient.

2811

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

2088

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