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Early clinical development


Eurasia Huizhi boasts more than ten Phase I strategic collaboration centers, providing high-quality, specialized resources for early-phase clinical studies of innovative drugs. For each project, our expert medical team drafts initial clinical study protocols, consults with clinical experts in relevant fields, and develops clinically feasible and regulatory-compliant implementation plans. The company has extensive experience in conducting clinical trials for a variety of new drugs, including chemical drugs, traditional Chinese medicines, and biologics. Our services include: 1) Feasibility Assessment: Clinical trial feasibility evaluation, identification of centers/researchers, and center feasibility assessment & qualification review. 2) Medical and Clinical Strategy & Planning: Clinical trial planning & execution, risk identification & management.

Early clinical studies serve as a bridge between preclinical research and translational medicine, linking them to clinical development efforts. By integrating existing clinical data, these studies help companies make informed decisions about product development.

Phase I, First-in-Human Trial

Phase IIa clinical study, Proof of concept

PK, PK/PD

Drug interaction study trials;

Food effect study trial;

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