HEALTH insurance reimbursement, SCIENTIFIC observation, DECISION making, DATA analytics, REPORTING of diseases, PHARMACEUTICAL industry, ACQUISITION of data, ELECTRONIC health records
Abstract
The article focuses on EMA's promotion of real-world data (RWD) in non-interventional studies for generating real-world evidence (RWE), addressing methodological aspects, governance, and data quality, aligning closely with FDA guidance but highlighting differences in NIS definitions, aiming to enhance regulatory decision-making and scientific rigor while improving transparency and reliability of industry-generated RWD.
DRUG approval, INSTITUTIONAL cooperation, INVESTMENTS, VACCINES, INVENTORY shortages, HEALTH services administration, SOCIAL support, GOVERNMENT regulation, NEGOTIATION, CELLULAR therapy, MANUFACTURING industries, MEDICAL supplies, DRUG packaging, ORGANIZATIONAL goals, BUSINESS networks, HEALTH insurance reimbursement, SUPPLY chains, PATENTS, INTELLECTUAL property, DRUGS, INTERPROFESSIONAL relations, QUALITY assurance, GENE therapy, DRUG labeling, COMMUNICATION, PHARMACEUTICAL industry, COVID-19 pandemic, PUBLIC opinion, PSYCHOLOGICAL resilience, MEDICAL research
Abstract
The article focuses on insights provided by Steffen Thirstrup, the chief medical officer at the European Medicines Agency, regarding regulatory challenges and successes in Europe's pharmaceutical landscape. Topics discussed include the impact of the COVID-19 pandemic on regulatory agility, challenges and collaborations in drug pricing and reimbursement, and efforts to enhance supply chain resilience and proximity to manufacturing infrastructure.
Published
2024
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