Answer Posted / bhalchandra

as per my evolution we check QC analysis related activity & found ok, then we check API & vendor found any other impurity is 0.03% (Limit is 0.2%) but after manufacturing I found any other impurity is 0.67% (Limit is0.5%)

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

2544

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when i come in contact with any metal items or clothes of fur i find myself shock and when run my fingers on fur clothes or matters, i find sparks. Is there any vitiams deffecieny in my body. If so, what i have to do?

2176

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

2195

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

2408

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

2098

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plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,

2397

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when we connect the capacitor banks in series with the circuit? 2 144 pH is having unit?

2207

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

2503

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please explain the job responsibilities of quality assurance..

2315

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How should the Medical Librarian interact with training staff?

2246

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what is factor?

2224

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Hi Sir?Mam, If i complete SAS CLINICAL in India, can i step forward to USA for job trials? How far is it possible? Am a B.pharm student ,willing to make up my Master's degree too,will this both M.Pharm and SAS help me out to get a job in USA? Please help me out with a good answer.

2128

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

2317

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How to perform forced degradation on tablet sample or suspensions?

1048

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what is the leak test procedure of filled bottles (liquid)

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