DIA Europe 2019 has ended

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DIA Europe 2019

13:30 CET

#PS02: Oral Poster Session 2 - Clinical Development & Pharmacovigilance Content Hub Content Hub 2

15:30 CET

#CHS04: Accelerating Clinical Study Start Up with Innovative Technologies Content Hub 2

10:15 CET

#CHS01: New Legislative Requirements in PV: How to Be More Efficient and Minimise Resources Content Hub 2

14:45 CET

#CHS04: Navigating the Regulatory Landscape for Safety Reporting in Clinical Trials: Key Principles, Best Practices, and Upcoming Automation Content Hub 2

15:15 CET

#CH201: Recent Developments and Possibilities in Using CPRD as a ‘Real World Data Source’ Content Hub 2

15:45 CET

#CH202: Collaborating to Solve the Industry’s Toughest Challenges: Maximizing the Regulator-Sponsor Relationship Content Hub 2

16:15 CET

#PS06: Oral Poster Session 6 - Clinical Development & Pharmacovigilance Content Hub Content Hub 2

09:15 CET

#CH203: Innovation in Pharmacovigilance Content Hub 2

09:45 CET

#CH204: Innovative Designs under the New Clinical Trials Regulations Content Hub 2

10:15 CET

#CHS05: Prudenta: An Electronic Solution for Local Literature Monitoring in Pharmacovigilance Content Hub 2

13:30 CET

#PS07: Oral Poster Session 7 - Clinical Development & Pharmacovigilance Content Hub Content Hub 2