define process validation

7 Answers  

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How do you fix the known and unknown impurity limit for a drug substance?

2 Answers   IBM,

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what are the limits for LOD and LOQ? should it be necessarily less than 1?

2 Answers   Cipla,

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difference between related substances and purity?

1 Answers   Micro Labs, Zydus Cadila,

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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.

0 Answers   Alchem, Getz Pharma Research, Hovid Berhad,

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Explain photostability ?

2 Answers   Lupin,

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IF We have to autoclave two chamber of media one having temp 100 c and onather at RT,which one get autoclaved first?

1 Answers  

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What are your intentions towards the uplift of the hospital.

0 Answers  

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

0 Answers   Claris Lifesciences,

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what are the principles of immunisation?

2 Answers  

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what is the diffirence between deviation and change control? at what situations we can raise the deviation and change control

31 Answers   Biocon, Cipla, DRL, Glenmark, Granules, Lupin, Micro Labs, Mylan, Natco, Ranbaxy, Swissmedic,

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

0 Answers  

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