MODULE 5: Manufacturing

module-5-manufacturing

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235038

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Facilities needed for pharmaceutical research:

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235039

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The production department of a pharmaceutical manufacturing establishment is in charge of, except:

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235040

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One of the ff. is not a QC function:

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235041

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Documentation is the main responsibility of:

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235042

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It means any establishment engaged in operations involved in the production of drugs including propagation, processing, compounding, finishing, filling, packing, repacking, and labeling in view of storage distribution or sale of the product:

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235043

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Statement of expiration date assure of:

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235044

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The expiration date of paracetamol tablet states January 1999. This statement means that, by January 1999, the product will have lost its activity:

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235045

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The barcodes imprinted in labels of products serve to:

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235046

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These are quality assurance functions, except:

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235047

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One of the ff. situations can avoid cross contamination and mix-ups:

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235048

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The manufacturing batch record should contain the ff. information, except:

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235049

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The QA inspectors usually inspect and audit warehouse CGMP’s :

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235050

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If a bottle of tablets has an expiration date of January 1999, the pharmacist may,

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235051

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Reaction kinetics study can help predict the:

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235052

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In the CGMP, we usually consider the:

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