Examples of 'bioequivalence' in a sentence
Meaning of "bioequivalence"
bioequivalence (noun): A pharmaceutical term used to describe the similarity in the absorption and concentration of two drug formulations, typically used to assess the efficacy and safety of generic medications against brand-name drugs
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- A measure of the equivalence of multiple formulations of a drug in terms of bioavailability
How to use "bioequivalence" in a sentence
Basic
Advanced
bioequivalence
For generic applications bioequivalence must be demonstrated.
Bioequivalence is a sine qua non to generic drugs.
Scientific advisory committee on bioavailability and bioequivalence.
Bioequivalence study in accordance with market requirements.
Use of group sequential design in bioequivalence studies.
Bioequivalence was established for none of the anthocyanins.
Such studies usually involve bioequivalence studies.
Bioequivalence assessments according to current guidelines were performed.
Pharmaceutical equivalence does not necessarily imply bioequivalence as.
Intraduodenal bioequivalence as compared to intravenous injection was determined.
Below is a general outline of an in vivo bioequivalence study.
A single bioequivalence study was conducted to support both applications.
Appropriate bioavailability studies shall be undertaken to establish bioequivalence.
Bioequivalence of vaporization compared to smoking has not been established.
Exemption from the requirement for bioequivalence studies.
See also
The bioequivalence studies are crucial in order.
Clinical data requirements are mainly pharmacokinetic bioequivalence studies.
Bioequivalence exists between the two dosage forms.
Design and monitoring of bioequivalence studies.
Bioequivalence may be demonstrated by in vivo and in vitro methods.
Automate bioavailability and bioequivalence studies.
The bioequivalence and therapeutic efficacy.
None of these subjects were included in the bioequivalence analysis.
Bioequivalence with the monocomponent products has been adequately demonstrated.
The demonstration of the bioequivalence with the reference product.
Bioequivalence between the test product and the originator.
Results of the bioequivalence studies.
Bioequivalence and safe switch.
Waiver from bioequivalence studies.
Bioequivalence and labelling of medicines with regard to generic substitution.
There was general discussion on bioequivalence requirements for these drugs.
Bioequivalence and generic drugs.
Cases for which certain bioequivalence studies were not relevant.
Bioequivalence had never been formally established between brands.
Investigation of bioavailability and bioequivalence.
Bioequivalence in the multiple dose study has not been sufficiently demonstrated.
The basis for registration of a generic drug is bioequivalence study.
Bioequivalence in fed conditions.
Pharmacokinetic parameters were calculated and bioequivalence evaluated afterwards.
Bioequivalence in fast conditions.
This method successfully concluded bioequivalence and its absence.
Bioequivalence and labelling of medicinal products with regard to generic substitution.
Understand the fundamental principles and benefits of bioequivalence testing.
Full bioequivalence study.
These clinical batches will be used in the bioequivalence study.
Bioequivalence may be demonstrated through several in vivo and in vitro methods.
Expert advisory committee on bioavailability and bioequivalence record of proceedings.
Bioequivalence studies usually form the basis for approval of generic medicines.
It must also demonstrate bioequivalence.
Bioequivalence of ketoprofen in swine was not observed between different routes of administration.
