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All stakeholders, including leaders across industry and health authorities, agree that finding answers to market access is critical to delivering breakthrough medicines to patients. Unfortunately, policies and practices do not always marry up.

This meeting will bring together professionals working with regulatory and value strategies. HTA bodies and regulators are breaking down silos, facilitating access to new promising medicines and increasing efficiencies in assessment processes. Similarly, R&D processes need to adapt to generate the appropriate evidence for registration and reimbursement that should allow patients’ timely access to innovative and promising drugs.

We are bringing together policy makers, developers, and the patients as end users, to keep you ahead of the game with practical solutions.

DIA shares insights in advance of this conference:

Hear a preview of programme committee member Solange Corriol-Rohou’s perspective on evidence generation throughout the life-cycle to support Medicines Adaptive Pathways to Patients (MAPPs) in the IMI project ADAPT SMART Webinar: ADAPT SMART “Putting Stakeholders at the Centre”

Featured topics

  • Acceptance of RWD by HTA bodies/payers
  • Early access to market
  • Definition of unmet medical needs
  • Alignment on evidence requirements across EU and between regulators and HTA
  • Methodologies for HTA and pricing of products in combination or multiple indications
  • Cross-functional multi-stakeholder dialogue to optimize market access and product affordability
  • Patient’s role in the regulatory and HTA process

Who should attend?

  • Professionals working in regulatory affairs and HTA/market access
  • Professionals involved in drug development, e.g. clinicians, epidemiologists and biostatisticians
  • Patient organisations
  • Biotech companies, drug developers including SMEs
  • Decision makers (Ministries of Health etc.)

Program Committee

  • Solange  Corriol-Rohou, DrMed, MD, PhD
    Solange Corriol-Rohou, DrMed, MD, PhD Senior Director, Global Regulatory Affairs & Policy, Europe
    Astrazeneca Research & Development, France
  • Angelika  Joos, MPharm
    Angelika Joos, MPharm Executive Director, Global Regulatory Policy
    Merck Sharp & Dohme (Europe) Inc., Belgium
  • Katarzyna  Kolasa, PhD
    Katarzyna Kolasa, PhD Professor of Health Economics, Head of Dept. of Health Economics and Health Mgmt
    Kozminski University, Poland
  • Mira  Pavlovic, DrMed, MS
    Mira Pavlovic, DrMed, MS HTA Expert / Managing Director
    NDA Advisory Services, Medicines Development and Training (MDT) Services, France
  • Claudine  Sapède, PharmD
    Claudine Sapède, PharmD Director, Global HTA Policy
    Novartis Pharma AG, Switzerland
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