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

2 Answers   Cipla,

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define process validation

7 Answers  

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what is meant by CAPA?what is the source for deviation (unplanned) to occur, though the process developed by standard validation procedures?

3 Answers   GSK GlaxoSmithKline,

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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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using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc?

1 Answers   Vivimed Labs,

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difference between related substances and purity?

1 Answers   Micro Labs, Zydus Cadila,

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exolain th function of the joints

2 Answers  

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If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration?

0 Answers   Cipla,

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Difference between Change control and Deviation please give the answer elaborately

1 Answers   Rakshit Drugs, Smilax,

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What is difference between Warm and Lukewarm Water as per pharmacopia.

0 Answers  

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

0 Answers   TATA,

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why use toline in resolution in uv calibration

1 Answers   Reddy Labs,

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