businessHosted by Regulatory Affairs Professionals Society (RAPS)
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This webinar examines how regulatory teams can coordinate ePI, eCTD v4.0, structured CMC, and related global submission requirements through a common governed content foundation. It addresses timelines across FDA, EMA and PMDA and explains how reusable structured content and traceability can reduce duplication and strengthen inspection readiness.
Date
Time
08:00 AMPlatform
Digital Hub
Global
Hosted By
Regulatory Affairs Professionals Society (RAPS)
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