アジェンダ
5:45 AM — 7:45 AM
Pre-Course Work – can be done at any time prior to the live event7:45 AM — 8:30 AM
8:30 AM — 9:00 AM
Session 1: Introduction and Welcome9:00 AM — 9:30 AM
Session 2: Drug Safety Jeopardy9:30 AM — 10:00 AM
Session 3: Lifecycle of Medical Product Safety10:00 AM — 10:15 AM
10:15 AM — 11:15 AM
Session 4: Clinical Trial Safety Regulations – US IND Safety Reporting11:15 AM — 12:00 PM
Session 5: CTTI Webinar12:00 PM — 12:30 PM
Session 6: FDA Guidance for Industry on Safety Reporting12:30 PM — 1:15 PM
2:00 PM — 3:00 PM
Session 8: Assessing Individual Case Safety Reports3:00 PM — 3:15 PM
3:15 PM — 4:15 PM
Session 9: SAE Case Study5:00 PM — 5:15 PM
Day One Wrap-Up/Questions and Answers7:30 AM — 8:00 AM
8:30 AM — 9:15 AM
Session 12: Overview of Case Processing9:15 AM — 10:00 AM
Session 13: Post-Marketing Safety Regulations – US10:00 AM — 10:15 AM
10:15 AM — 10:30 AM
Session 14: EMA Web Site10:30 AM — 12:00 PM
Session 15: Post-Marketing Safety Regulations – EU12:00 PM — 1:00 PM
1:00 PM — 2:00 PM
Session 16: Aggregate Reporting for Marketed Products2:45 PM — 3:00 PM
3:00 PM — 3:30 PM
Session 18: FDA Warning Letters3:30 PM — 4:15 PM
Session 19: Individual Case Safety Reports4:15 PM — 5:15 PM
Session 20: Spontaneous Case Report5:15 PM — 5:30 PM
Day Two Wrap-Up/Questions and Answers5:30 PM — 7:30 PM
7:30 AM — 8:00 AM
8:00 AM — 8:45 AM
Session 21: Review the Reporting Matrix Worksheet8:45 AM — 9:45 AM
Session 22: Safety Data Coding9:45 AM — 10:15 AM
Session 23: MedDRA Coding10:15 AM — 10:30 AM
10:30 AM — 11:45 AM
Session 24: Introduction to Signal Detection11:45 AM — 12:45 PM
12:45 PM — 1:45 PM
Session 25: Benefit-Risk Management1:45 PM — 2:00 PM
Session 26: REMS@FDA Web Site2:00 PM — 2:15 PM
2:15 PM — 2:45 PM
Session 27: MedWatch Learn2:45 PM — 3:30 PM
Session 28: Organization of the Safety Department3:30 PM — 4:00 PM
Course Wrap-Up/Questions and Answers