why use toline in resolution in uv calibration

1 Answers   Reddy Labs,

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IF We have to autoclave two chamber of media one having temp 100 c and onather at RT,which one get autoclaved first?

1 Answers  

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

1 Answers  

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How to set impurity limits for Related substances test.

1 Answers  

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How should the Medical Librarian interact with training staff?

0 Answers  

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How do you fix the known and unknown impurity limit for a drug substance?

2 Answers   IBM,

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why an employee go for medical representative instead of quality?

1 Answers  

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How to perform forced degradation on tablet sample or suspensions?

0 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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Which types of deviations are followed in pharmaceuial API manufacturing industry?

1 Answers   Laurus,

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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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diffrence between known impurity and specified impurity?

2 Answers   Cipla, Medreich,

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