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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

Drug quality control

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Pharmacovigilance (building a pharmacovigilance system, safety in clinical trials, pharmacovigilance audit, pharmacovigilance contact persons)

Conducting patient leaflet user testing

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