EU Joint Clinical Assessment Poster Tour
Speaker(s)
Melinda Goodall, MSc PhD, Goodall HTA Consulting, Manchester, Manchester, UK
Presentation Documents
Posters featured in this tour:
- PT25: Comparison of Approval Dates of New Substances between the United States of America (FOOD AND DRUG ADMINISTRATION, FDA) and Europe (EUROPEAN MEDICINES AGENCY, EMA)
- PT26: How Aware Are Biotech and Pharmaceutical Companies of the Implementation of the New EU HTA?
- PT27: How Much Does TLV Value Rarity? A Review of Reimbursement Decisions on Orphan Drugs in Sweden from 2017 through 2022
- PT28: Lost in PICO? a Simulation of the EU HTA Scoping Process
- PT29: Predicting PICOs for EU Joint Clinical Assessment: Lessons from PICOs in Relative Effectiveness Assessments (REA) from EUnetHTA Joint Action 3 Project
- PT30: Will Health Technology Assessment (HTA) Bodies in Europe Accept Evidence from an External Control Arm to Supplement Evidence from Clinical Trials for Chronic Diseases?
Code
212