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Bioavailability testing criteria

Although different standards are set for different classes or types of drugs, the general bioavailability standard is an upward or downward variation of no more than 20%. Most generic versions tested to date have demonstrated plasma levels within 3% to 5% of the innovator drug. Sentiment is growing for an achievable +10% bioavailability criterion. [Pg.58]

Figure 4. Bioavailability of monoferric phytate baked into bread. Rats were the test species and change in hemoglobin concentration during a 2-week repletion period was bioassay criterion. Figure 4. Bioavailability of monoferric phytate baked into bread. Rats were the test species and change in hemoglobin concentration during a 2-week repletion period was bioassay criterion.

See other pages where Bioavailability testing criteria is mentioned: [Pg.3191]    [Pg.75]    [Pg.102]    [Pg.109]    [Pg.430]    [Pg.10]    [Pg.217]    [Pg.21]    [Pg.311]    [Pg.50]    [Pg.1603]    [Pg.204]    [Pg.321]   
See also in sourсe #XX -- [ Pg.100 ]




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