What are the regulatory commitments in markets like USA,
Canada, Europe, Brazil, South Africa and Japan
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Can any one tell me that which brand hplc column is used for levetiracetam imp- b test.
why we have to use only 900 ml buffer in dissolution apparatus ? what are the conditions that favours the selection of volume of buffer?
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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,
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,
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