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Storage labelling

While the majority of critical manufacturing operations of injectable pharmaceuticals (e.g. most biopharmaceuticals) occurs in specialized clean areas, proper design and maintenance of non-critical areas (e.g. storage, labelling and packing areas) is also vital to ensure overall product safety. Strict codes of hygiene also apply to these non-critical areas. [Pg.97]

Written sampling plans Representative samples Authenticity of batch information provided Storage, labeling, transferring, and tracking of samples Testing... [Pg.219]

Ail handling of materials and products, such as receipt and quarantine, sampling, storage, labelling, dispensing, processing, packaging, and distribution should be done in accordance with written procedures or instructions and, where necessary, recorded. [Pg.33]


See other pages where Storage labelling is mentioned: [Pg.237]    [Pg.1223]    [Pg.86]    [Pg.1962]    [Pg.578]    [Pg.185]    [Pg.64]    [Pg.141]    [Pg.541]    [Pg.430]    [Pg.227]    [Pg.3]    [Pg.4]    [Pg.5]    [Pg.7]    [Pg.9]    [Pg.10]    [Pg.12]    [Pg.16]    [Pg.19]    [Pg.23]    [Pg.24]    [Pg.25]    [Pg.27]    [Pg.28]    [Pg.29]    [Pg.30]    [Pg.31]    [Pg.32]    [Pg.36]    [Pg.37]    [Pg.40]    [Pg.41]    [Pg.42]    [Pg.43]    [Pg.46]    [Pg.49]    [Pg.50]    [Pg.51]    [Pg.52]    [Pg.54]    [Pg.56]    [Pg.58]    [Pg.61]    [Pg.63]    [Pg.64]   
See also in sourсe #XX -- [ Pg.459 , Pg.815 ]




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Labels storage instructions

Stability storage labels

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