DATA SEARCH AND ANALYSIS

X7 Research team conducts an independent expert review of documents (physicochemical report, in-vitro, in-vivo, toxicity, immunogenicity, local tolerance, clinical study reports) for compliance with regulatory requirements of Russia, EAEU, CIS, EU.

If it is possible to register drugs on the basis of literature reviews on preclinical and clinical studies, the scientific department of X7 Research performs a qualitative and quantitative assessment of the sources to prepare a full-fledged document.

CONDUCTING A GAP ANALYSIS

LITERATURE REVIEW

DOCUMENT REVIEW

X7 Research has extensive experience in finding and analyzing drug-specific information to prepare a drug registration strategy in Russia, EAEU, CIS, EU

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