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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Tolerance limit for dissolution media rpm sampling point.

1 Answers   Torrent Pharma,

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How to set impurity limits for Related substances test.

1 Answers  

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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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what is the disintegration time of mouth dissolving tablet

3 Answers   Unimarck Pharma,

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WHAT IS MEANING OF DEAIATION WITH EXAMPLE

0 Answers   KarMic,

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please explain the job responsibilities of quality assurance..

0 Answers  

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diffrence between known impurity and specified impurity?

2 Answers   Cipla, Medreich,

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What is difference between Analytical method validation and Analytical method transfer?

4 Answers   Apotex,

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Job oriented Training in Oracle Clinical, CDM, Clinical Research and SAS with Clinical Trails

1 Answers  

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What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets

0 Answers  

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What experience do you have in training?

0 Answers  

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