Explore the 2018 Programme
-
2018 Programme Highlights
Following the encouraging attendee responses from 2017, we are continuing to include both the successful DIAmond Sessions and the Rapid Fire Closing Session.
DIAmond Sessions: The comprehensive sessions are held Tuesday-Thursday, and include 10 global hot topics with regulatory, payer, industry, and patient perspectives. These panel conversations are can’t-miss opportunities to listen to and engage with diverse stakeholders involved in each topical area.
Rapid Fire Closing: This must-attend ‘Rapid Fire’ session is an excellent opportunity to hear what you may have missed during the sessions you were unable to attend! All Session Topic Leaders will have 3 minutes onstage to share summaries of novel insights and key takeaways from the DIA Europe 2018.
-
New for 2018 Programme
In 2018 we are introducing new sessions designed to facilitate dialogue and connect with more directly with the right content and the right people.
DIAlogue Sessions: These are dynamic, outcome-focussed sessions where stakeholders converge to solve a real problem. Preparatory groundwork will be laid out by the session organisers and presented to the audience as a preface to interactive discussion.
Content Hubs: Presentations will be led by DIA members in an informal setting. Engage with fellow attendees who have designed a 30-minute interactive exchange that will offer you rapid insight in a subject of value, or a deeper perspective of a compelling session given earlier in the meeting.
Engage & Exchange (E&E): Share ideas, exchange experiences, and enhance your understanding of a topic that’s important to you! Actively participate in this collaborative learning environment, with a 45-minute session led by a facilitator.
-
2018 Programme Topics
The 2018 Programme Topics are:
- Topic A: Can Regulators and HTA Bodies Create Synergies for Patient Access?
- Topic B: What are Necessary Steps towards Outcome-Driven Health Systems?
- Topic C: Medicines of the Future: What Will Innovation Need and Bring?
- Topic D: How Can Better Outcomes Be Enabled by Big Data?
- Topic E: What is the Future of Pharmacovigilance?
- Topic F: What Can Stakeholders Expects from Clinical Trial (Development), Transparency and Medical Information?
- Topic G: A New Era for Medical Devices and Diagnostics. How Is The Impact?
- Topic H: Drug Development and Regulatory Approval - Reference Points around the Globe or Globalisation?
- Topic I: How Can We Enable Clinical Research in Europe Further?