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Swissôtel Le Plaza

2019年10月24日 (木) 午前 9:00 - 2019年10月25日 (金) 午後 5:30

Messeplatz 25, 4005 Basel, Switzerland

Value, Access & Regulatory Evidence Workshop

Acknowledging the different perspectives and finding the pragmatic way forward

Session 4: Post Licensing Evidence Generation – What Is It and What Is Its Purpose?

Session Chair(s)

Niklas  Hedberg, MPHARM

Niklas Hedberg, MPHARM

HTACG Co-Chair & Chief Pharmacist

Dental and Pharmaceutical Benefits Agency, TLV, Sweden

Post Licensing Evidence Generation – What Is It and What Is Its Purpose?

Speaker(s)

Irena  Guzina, PHARMD, MPH, MSC

How the PLEG Landscape Has Changed in the Past Decade – EUnetHTA perspective

Irena Guzina, PHARMD, MPH, MSC

HAS, France

Medical Assessor, Coordinator of EUnetHTA WP5B PLEG Activities

Peter  Mol, PHARMD, PHD

Current Challenges and Gaps in PLEG and Their Implications for Regulatory and Reimbursement Decision Making

Peter Mol, PHARMD, PHD

MEB, Netherlands

CHMP member, NL

Michael  Berntgen, PHD

Utilising Different Data Sources for Post-Licensing Evidence – Opportunities and Challenges

Michael Berntgen, PHD

European Medicines Agency, Netherlands

Head of Scientific Evidence Generation

Catherine  Cohet, PHD

PLEG: The Perspective of Pharmaceutical Developers

Catherine Cohet, PHD

European Medicines Agency, Netherlands

Senior Pharmacoepidemiologist, Data Analytics and Methods Task Force

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