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Clinical Development & Regulation
Our team has extensive experience in conducting global clinical trials in America, Europe, Australia, and China, meeting different regulatory requirements. These experiences include clinical protocol design, orphan indication, pediatric application, clinical CRO management and process control, and IND and BLA filing. We have an established network of clinical experts including KOLs and regulatory experts helping the formulation of the clinical development and regulatory strategies for iTAb drug development.

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