15 years of practical experience in the field of clinical trial regulations in the EU/Australia/UK, specializing in CTIS system architecture and multinational team management. He is an authoritative expert in EU CTR 536/2014 and 2024/1938 regulations. Among an international pharmaceutical company, it leads the development of the Veeva system CTR content program, covering 20+ global multi-center research.
Looking ahead, we will continue to strengthen technological innovation and service upgrading, promote the healthy development of the pharmaceutical industry, and create greater value for customers. We look forward to cooperating with global customers to create brilliance together.
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Sophia.huang@brilliantmed.cn