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BUILD BETTER REGULATORY SUBMISSIONS WITH INDUSTRY CASE STUDIES, SPOR BEST PRACTICE AND FEEDBACK FROM REGULATORY AGENCIES

Optimise your global submissions strategy

A wealth of eCTD knowledge from around the world
  • Outlining the latest updates from Canada
  • Regulatory submission status in Jordan
  • eCTD developments in Singapore
  • Creating a global dossier plan for fast-tracking approvals
Take command of your EU Telematics plan
  • Best practices for implementing eCTD for National Procedures
  • Feedback and practical advice from a Regulatory Agency perspective
  • Updates and timelines on Clinical Trial Regulation and the Falsified Medicines Directive
Are you ready for SPOR? We’ve got you covered...
  • The latest on the SPOR implementation plans and timelines
  • Solidify your understanding and expectations for CESSP Phase 1
  • Benchmark your regulatory practices with peers from Submissions and Information Management