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Three days, three tracks at one location: Regulatory Data Management and Submissions; Regulatory in Emerging Markets and European Affairs
Day One: Bringing the data management and eSubmissions worlds together... Are you ready?
- Regulatory Information Management Day
- Regulatory Submissions and Management Joint Day
- Submissions Day
Day Two: Indistry leaders guide you thoruhg submissions in Asia
Day Three: Regulation requirements review to ensure you stay on top on your game – Brexit, Clinical Trial Regulation and GDPR
WHO ATTENDS:
2,000 attendess from the medical device and pharma space: Regulatory Affairs and Operations; Regulatory Information Management; Global Submission/Project Management; Medical, Technical, and Regulatory Writing Data Management; Information Technology and Support; Document and eRecords Management;
