| The requirements for data disclosure in clinical trials are continuously evolving. Although the purpose is to ultimately make data transparency greater, the constant updates can make it hard to understand what the current regulations are and what are coming up. This leads to many questions, including what data submissions are requirement for certain trials? What are the implications of the new EU regulation and the US expanded rulemaking? How do these regulations impact the running of future clinical trials?
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ArisGlobal to Discuss AI Enabled Data Fabric and Emerging Pharmacovigilance Technologies at World Drug Safety
The life sciences R&D technology leader will lead keynote sessions on both days of World Drug Safety Boston Miami, FL October 20, 2021 - ArisGlobal, the leading provider of software that automates core product development functions for over 300 global life...