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

Health Pharma Interview Questions

Questions Answers Views Company eMail

what is difference between humidity and relative humidity

Cipla,

1 7977

what do you mean by mean kinetic temperature in stability

2 16991

what do you mean by bracketing and matrixing in stability

1 6346

how to select HPLC column for a particular product

3953

what is the composition of C18 column

Cipla, Deccan,

2 26327

what is limit of cleaning validation

2500

what is recovery factor

Jubilant,

2220

how much the minimum recovery should be in swab sampling

1 13078

what do you mean by Q+5 in dissolution

1 25238

what is difference between in drug purity and drug potency

2 5291

what should be minimum limit of working standard

1 18731

how impurity is analyzed in a tablet

3451

what is difference between method validation and method verification

1 3893

what should be the LOD of dry syrup

1 8047

how you can fix the known and unknown impurity limit for any drug substance

3223

Un-Answered Questions { Health Pharma }

What is column efficiency and performance ? And how can we know the column is better?

1790

What is Calibration Curve?

1193

why we use matrixing method in stability study and on what basis time points are selected?

2058

What is the role of buffers (ex: KH2PO4) in HPLC analysis,

1714

why we use SLS in dissolution

943

What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets

4414

how the qualification of pharma can help in banking

2158

what is the calculation for getting the tablet weight and the punch size, Eg..if there is a 8/32 punch then how to measure tablet weight????

5755

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

2546

What is the difference between polarimeter lamp and IR lamp?

5633

What is your work experience in pharmaceutical field?

1112

What is main of k*abs in uv visible spectroscopy

2202

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

2720

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

2361

Why and When RRF is necessary in RS method? How it is helpful in method development?

2231

For More Un-Answered { Health Pharma } Questions Click Here