グローバル臨床試験情報開示の基本 – 要件、タイミング、違反時の影響

開示の基本要件について、オンデマンドウェビナーでご確認いただけます。何を、いつ、どのように開示すべきか。規制の執行メカニズムや、コンプライアンスを維持することがなぜ重要なのかについても学べます。

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特別講演者

Ben Evans

Disclosure Regulations Research Manager, Citeline

Ben Evans leads the development and evolution of TrialScope Intelligence, a global clinical trial regulatory intelligence platform that delivers high-quality, actionable content to help clients navigate complex disclosure regulations. His role combines research, strategy, and cross-functional collaboration, working closely with regulatory experts, product, tech, and commercial teams to ensure alignment with client needs and company goals.