Overview
Europe is facing challenging discussions related to affordability and patient access. Ongoing collaboration activities between national HTAs and between HTAs and Regulators hold some promise for better alignment of requirements that will allow more predictable assessment outcomes in Europe. Stakeholders have started to dialogue across disciplines and legislators are proposing new instruments to set up a sustainable system for EU collaboration on clinical value assessments. This meeting highlights the most recent advances on hot topics touching the interface between regulatory and patient access by providing perspectives from different stakeholders.
The meeting is a must-attend for anyone working on innovative solutions in clinical development, regulatory, access, outcomes research or health policy. It gives the opportunity to directly ask your burning questions on regulatory and patient access strategy topics to patients, scientists, policymakers, regulators, payers and HTA bodies.
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Program Committee
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Angelika Joos, MPharm Executive Director, Global Regulatory Policy
MSD, Belgium -
Mira Pavlovic, DrMed, MD, MS HTA Expert /Director/HTA Professor
NDA Advisory Services, Medicines Development and Training (MDT) Services, France -
Claudine Sapède, PharmD Director, Global HTA Policy
NOVARTIS INTERNATIONAL, Switzerland -
Olga Solomon, MS Head of Unit B5 - Medicines: Policy, Authorisation and Monitoring
European Commission - DG SANTE, Belgium -
Kristin Svanqvist, MPharm Governmental Affairs Manager
Amgen, Norway -
Solange Corriol-Rohou, DrMed, MD, PhD Senior Director, Global Regulatory Affairs & Policy, R&D, Europe
AstraZeneca , France -
Katarzyna Kolasa, PhD Professor of Health Economics, Head of Dept. of Health Economics and Health Mgmt
Kozminski University, Poland
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