Health Pharma AllOther Interview Questions, Answers for Freshers and Experienced asked in various Company Job Interviews

Health Pharma AllOther Interview Questions

Questions Answers Views Company eMail

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

Laurus,

1 4480

What are the significance of MKT in stability study.

Alembic,

1 7466

What is the different between GMP & cGMP ?

1 7586

what is the mechanism of action of local anaesthetics?

2292

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 7190

what is the disintegration time of mouth dissolving tablet

Unimarck Pharma,

3 7861

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

2 7027

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

2612

please explain the job responsibilities of quality assurance..

2388

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,

2713

How to set impurity limits for Related substances test.

1 4714

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

Vivimed Labs,

1 3503

Tolerance limit for dissolution media rpm sampling point.

Torrent Pharma,

1 3970

diffrence between known impurity and specified impurity?

Cipla, Medreich,

2 7059

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

Lupin, Teva Pharmaceuticals,

2554

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Un-Answered Questions { Health Pharma AllOther }

Give an example of how you've handled a problem patient.

2455

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

2363

What r the different sop in or plant

1991

You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.

2149

What is forced degradation study?

1259

How to preform dissolution profiling

1984

Explain difference between sonication and homozinization?

1104

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

1537

How can I assign a retest date for solvents e.g. toluene, methanol, etc?

3049

What are your intentions towards the uplift of the hospital.

2143

Can any one tell me that which brand hplc column is used for levetiracetam imp- b test.

1882

How to perform forced degradation on tablet sample or suspensions?

1119

What is the basic requirement for preparing drug master file , like EDMF , USDMF ?

2776

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

2678

What was your most difficult experience with this population and how did you deal with it?

2206

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