Examples of 'comparative bioavailability' in a sentence
Meaning of "comparative bioavailability"
This term is used in pharmacology to describe the extent and rate at which a drug is absorbed into the bloodstream and becomes available to produce its desired effect, in comparison to other drugs or formulations
How to use "comparative bioavailability" in a sentence
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comparative bioavailability
Comparative bioavailability of ranitidine tablets and suspension.
Summary table of the comparative bioavailability data.
Comparative bioavailability study.
Bloequlvalence and comparative bioavailability studies.
O Certificates of Analyses for test and reference products used in a comparative bioavailability study.
This is known as a comparative bioavailability study.
Comparative Bioavailability Studies A comparative bioavailability study was performed using healthy human volunteers.
This guidance applies to all comparative bioavailability studies.
Biowaivers for comparative bioavailability studies in support of Drug Identification Number ( DIN ) Applications.
This comparison is usually done through comparative bioavailability studies.
Determination of comparative bioavailability should be based on data for the parent drug.
O waiver requests in relation to conducting a comparative bioavailability study.
Bioanalytical Methods A comparative bioavailability study in beagle dogs was performed on ten female animals.
This manufacturing site transfer is a significant change that requires a comparative bioavailability study to support it.
The following comparative bioavailability standards should be met,.
See also
Health Canada determines bioequivalence based on comparative bioavailability studies.
The following standards in a comparative bioavailability study will be used to determine bioequivalence, 1.
The cross-over design is the preferred design for comparative bioavailability studies.
Figure 1 represents comparative bioavailability study of different pharmaceutical compositions of curcumin in rats ( n=6 ).
Some drugs are not suitable for comparative bioavailability testing.
Comparative bioavailability of EPO after S.C. administration.
We reiterate that this notice applies to comparative bioavailability ( bioequivalence ) studies only.
Comparative Bioavailability Studies ( if required ).
For human pharmaceutical drugs the following comparative bioavailability standards should be met,.
O the number and type ( s ) of comparative bioavailability studies conducted, and whether any waivers were granted ;.
O T4 alone should be used as a measure of comparative bioavailability.
Bioequivalence ( CS, BE ) for pivotal comparative bioavailability ( bioequivalence ) studies should be included in this subsection.
O related Health Canada guidances and notices on Quality and comparative bioavailability information2.
We reiterate that this notice applies to comparative bioavailability ( bioequivalence ) studies involving combination products.
Requests for waivers and justification statements should be in provided in Module 1.6.1 Comparative Bioavailability Information.
The following standards obtained in single dose cross-over comparative bioavailability studies determine bioequivalence, 1.
O batch ( es ) used in the nonclinical, pivotal clinical and / or comparative bioavailability studies ;.
O What dose should be studied in a comparative bioavailability study?
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Examples of using Bioavailability
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Comparative bioavailability of ranitidine tablets and suspension
Scientific advisory committee on bioavailability and bioequivalence
The bioavailability is not affected by food intake
