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What is forced degradation study?
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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,
Why 3 validation batches charge in stability ?is there any specific reason for 3 ?
why an employee go for medical representative instead of quality?
my wife is Pregnant and in scanning report their is a mark ( + )what is that mean?
What interests you about the position of Medical Librarian in our company?
What is difference between Warm and Lukewarm Water as per pharmacopia.
What is forced degradation study?
exolain th function of the joints
What is the different between GMP & cGMP ?
Tell us about a situation in which you took the extra step for a patient.
0 Answers Claris Lifesciences,
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
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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