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Consulting (search and analysis of information, development of a registration strategy, assessment of the feasibility of a study, selection of vendors, budgeting).

Clinical studies (therapeutic equivalence, pharmaceutical equivalence, biological equivalence)

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Post-registration study

About us

The first Clinical Center for Bioequivalence, on the basis of which it is planned to conduct the clinical and biopharmaceutical parts of a clinical trial and provide manufacturers a full range of bioequivalence services, therapeutic equivalence, biowaiver studies within the EAEU at below market prices.

Kazakhstan’s 1st accredited Full Service CRO for bioavailability/bioequivalence

Providing a Self-sustaining Clinical Research ecosystem

Enabling Market Authorization beyond the EAEU

The first joint

Kazakh-Malaysian clinical center

offers the following benefits

when conducting bioequivalence studies:

Extensive database of volunteers

Quick recruitment of all study subjects

Rapid screening of volunteers

Simultaneous hospitalization of all study subjects

Well-established staff work and well-established procedure for blood sampling from volunteers

Standardized study conditions

 Standardized meals for volunteers

Dedicated team of researchers and nurses

 Ability to perform the most complex procedures

Expertise of research documents at the initial stage of their development

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