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Answer Posted / anuj sharma
GMP:-"Good manufacturing practice" or "GMP" is part of a
quality system covering the manufacture and testing of
active pharmaceutical ingredients, diagnostics, foods,
pharmaceutical products, and medical devices. GMPs are
guidelines that outline the aspects of production and
testing that can impact the quality of a product.
GLP:-GLP generally refers to a system of management
controls for laboratories and research organizations to
ensure the consistency and reliability of results.
ANUJ SHARMA
IPQA, INDSWIFT LABS CHANDIGARH
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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.
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