DIA has decided to change the format of the upcoming DIA Regulatory Science Forum from "face-to-face" (in-person) to entirely virtual.
This valuable forum WILL continue and be extended on the following dates, 28-30 September, in an entirely virtual meeting format, with both speakers and attendees participating remotely via a digital platform. More details will be provided in the coming weeks.
DIA’s mission – to work across the healthcare continuum to ensure patients receive the therapies they need – is more essential than ever during times like these. DIA acknowledges the time and effort that has gone into planning and preparing for the Forum, and trusts that everyone will understand the need to respond to current, evolving health concerns in a responsible manner. These precautions are being taken to ensure the health and safety of our entire, global DIA family.
DIA is committed to exploring all possible avenues to provide a productive setting and a fulfilling meeting experience. We appreciate your patience as we work through technical requirements and any potential challenges.
The Regulatory Science Forum is a platform for sharing knowledge derived from regulatory science research and analyses conducted at the academic, industry and regulatory levels, promoting open dialogue between all stakeholders. The Forum will discuss where more research is needed, as well as the best ways to promote the widespread implementation of findings, recommendations, and other results.
• Regulatory Science Training and Network in European Academia
• Maximizing the Value and Impact of Regulatory Science Research
• HTA-Regulatory Cooperation
• Stakeholder & Patient Engagement
• Body of Evidence
• Complex Clinical Trials
Who should attend?
Professionals involved in:
- Regulatory Science
- Regulatory Strategy
- Regulatory Intelligence
- Scientific Advice
- Data analysis
- Patient Engagement
By attending this meeting, participants will be able to:
• Become aware
Marieke De Bruin, PharmD, PhD • Director, Copenhagen Centre for Regulatory Science
University of Copenhagen, Denmark
Sini Eskola, MPharm, MSc • Director Regulatory Affairs
European Federation of Pharmaceutical Industries and Associations (EFPIA), Belgium
Helga Gardarsdottir, DrSc • Associate Professor in Drug Regulatory Sciences
Utrecht University, Netherlands
Anthony Humphreys, MPharm • Head of the Regulatory Science and Innovation Task Force
European Medicines Agency, Netherlands
Anne Vinther Morant, PhD, MSc • Regulatory Science Consultant
Anne Morant Consulting, Denmark
Marjon Pasmooij, PhD • Science Programme Manager
Medicines Evaluation Board, Netherlands
Sara Torgal • Scientific Programmes Manager
Aimad Torqui • Director Global Regulatory Policy
MSD, the Netherlands, Netherlands