Answer Posted / darose

information on drug substance- API (DMF)+ EXCIPIENTS
INFORMATION ON FINISHED PRODUCT, MANUFACTURING AND PACKAGING
(CMC)
INFORMATION ON DEVELOPMENT (R&D)
INFORMATION ON STABILITY OF FINISHED PODUCT
LABELING

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

2665

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Iam a B.PHARMA GRADUATE from DELHI UNIVERSITY and I am looking forward for DRUG INSPECTOR EXAM..kindly mail me any ques papaers reg the same...

2265

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How to preform dissolution profiling

2063

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why didn't you go back to previous employer after shifting to bangalore?

2325

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please explain the job responsibilities of quality assurance..

2434

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

2405

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What do you mean by GTT? What are the effect of GTT on film coating.

1707

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What interests you about the position of Medical Librarian in our company?

2621

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

3330

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

3087

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

2593

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concomitant administration of 6-mercaptopurine and which product results in severe bonemarrow suppression?

2718

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

2031

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Explain difference between sonication and homozinization?

1154

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Why SLS used as dissolution medium

1189

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