Saturday, 24 May 2014

Frequently asked questions in Pharmaceutical QA Interview



Q. Brazil falls under which climatic zone ?
Q. According to WHO guidelines what is the storage condition of climatic zone IVa and zone IVb?
Q. What is dead leg?
Q. Brief about ICH stabilty guidelines?
Q. What is significant changes in stability testing?
Q. Why do we check hardness during inprocess checks?
Q. Which type of tablets are exempted from Disintegration testing?
Q. What needs to be checked during inprocess QA checks?
Q. In a tablet manufacturing facility ‘positive’ pressure is maintained in processing area or service corridors?
Q. If sticking observed during tablet compression what may the probable reason for the same?
Q. Why do we consider three consecutive runs/batches for process validation? Why not two or four?
Q. Why do we calibrate a qualified equipment/instrument on definite intervals?
Q. What needs to be checked during AHU validation?
Q. What is the difference between calibration and Validation?

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