THERAPEUTIC EQUIVALENCE STUDIES

A therapeutic equivalence study is a type of clinical trials, which is carried out to identify the identical properties of medicinal products of a particular dosage form, as well as the presence of the same safety and efficacy of medicines, the same clinical effects during their use. Therapeutic equivalence is the main requirement for drug interchangeability. When planning a clinical trial of therapeutic equivalence, the main task is to justify the boundaries of equivalence recognition with the further use of statistical procedures to prove the value of the confidence intervals of differences within these limits.

X7 Research offers its clients full accompaniment and support at all stages of generic in Russia, EAEU, CIS, EU. We conduct therapeutic equivalence studies by current regulations.

EXPERIENCE IN ALL THERAPEUTIC AREAS

SUPPORT AT ALL STUDY STAGES

PROVIDING OWN CLINICAL SITE

The X7 Research team of professionals has decades of experience in conducting therapeutic equivalency studies. With our help, the report will successfully pass all necessary regulatory approvals.

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