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DIA Europe 2019

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08:30 CET

#KN3: Health Systems: Doomed to Fail or About Be Saved by a Copernican Shift? E1

09:15 CET

#CH104: Patient-reported, Patient-relevant, Patient-centred outcomes: definitions, roles and importance for health technology assessment Content Hub 1 #CH203: Innovation in Pharmacovigilance Content Hub 2 #CH305: Data’s Revenge Content Hub 3 #S0105: Opportunities in Regulatory System Optimisation - How to Maximise the Benefit? E1 #S0205: Orphan and Paediatric Medicines – Future Direction and Regulatory Landscape G1 #S0905: Converging Global Life Science Regulation – Where Are We Heading in 2025? K1 #S0305: GVP Module V Risk Management Plan: Lessons Learned One Year after the Revision 2 E2 #S0405: Reducing Cost and Improving Quality of Clinical Trials F1 #S0505: How to Extend MSL Expertise to Patient Engagement Activities G2 #S0705: Can We Improve Patient Experience with Digitisation – Part 1: Patient Information F2 #S0805: China - Update on the Regulatory Environment K2 #S0605: How to Facilitate Access to Advanced Therapy Medicinal Products in Europe DIAlogue Space #WS01: Automatic Translations Workshop 0.11-0.12 (Level 0)

09:45 CET

#CH105: Pilot Study Exploring Routes of Plain Language Summary Development: In Search of Efficiencies and Optimum Quality Content Hub 1 #CH204: Innovative Designs under the New Clinical Trials Regulations Content Hub 2 #CH306: Can the Efficacy and Quality of Medical Coding Be Improved by the Use of Artificial Intelligence? Content Hub 3 #CH407: Coping with a Medicine Mid-Life(Cycle) Crisis: Future Opportunities and Challenges in the Management of Post-Licensing Change Content Hub 4

10:15 CET

#CHS05: Prudenta: An Electronic Solution for Local Literature Monitoring in Pharmacovigilance Content Hub 2 #CB4: Coffee Break in the Exbition Hall Exhibition Hall

10:45 CET

#S0106: Regulatory Data Use and Integrity across Stakeholders E1 #S0206: Regulatory Innovation: Regulatory Science G1 #S0306: Risk Communication: New Directions for the Future E2 #S0406: Will Patient Involvement Improve Clinical Research? F1 #S0606: Precision Medicine into Action: The Case of a Histology Independent Label - What Implications for Value Assessment? DIAlogue Space #S0706: Can We Improve Patient Experience with Digitisation – Part 2: Digital Devices F2 #S0806: The Eurasian Union - Reflection on the Changes in Regulatory and Ways of Working K2 #S0906: ICH Info Day – Part 1 K1 #LOT05: Patient Advocacy, Next Generation of Young Patient advocates and Why Patient Advocacy Matters 0.96-0.97 (Level 0)

12:00 CET

#S0107: Comparing Apples with Oranges: How EU and US Expedited Regulatory Pathways Differ in Practice - Learnings, Reflections and Future Trends E1 #S0307: Capacity Building and Capability Building in Pharmacovigilance E2 #S0407: What Do These Buzzwords Mean – for Me? Artificial Intelligence, Big Data Mining, Machine Learning, Quantum Computing… DIAlogue Space #S0507: Hey Siri, I Am Not Feeling Well Today G2 #S0607: Assessing the Value of a Cure: Are HTA Approaches and Payment Models Fit for Purpose? G1 #S0707: Preparing the Way for a Learning Healthcare Ecosystem F2 #S0807: Strengthening the Supply Chain to Improve Access to Medicines in Africa K2 #S0907: ICH Info Day – Part 2 K1

13:15 CET

#L3: Lunch in the Exhibition Hall Exhibition Hall

13:30 CET

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

14:00 CET

#DMD10: Raising Europe’s Voice in Globalising Regulatory Science E2 #DMD11: Modern Clinical Research and Paradigm Shift – What Can We Take Home? F1

15:15 CET

Conference Closer- Rapid Fire Session F2