EMA-HTA Parallel Scientific Advice: Challenges and Opportunities - Fuchs, Ulrike
26,99 €
inkl. MwSt.
Versandkostenfrei*
Versandfertig in 6-10 Tagen
payback
13 °P sammeln
  • Broschiertes Buch

Compared to regulatory agencies - focusing on the benefit/risk assessment of a product, typically evaluated in the strictly controlled setting of randomized controlled trials with close attention to internal validity, safety, efficacy and manufacturing - HTA bodies have different remits and, therefore, additional evidence requirements. Criteria for reimbursement decisions vary across countries but can include unmet medical needs, the relative effectiveness and safety of the drug, drug price, budget impact and cost-effectiveness. Designing a study suitable for regulatory approval might not…mehr

Andere Kunden interessierten sich auch für
Produktbeschreibung
Compared to regulatory agencies - focusing on the benefit/risk assessment of a product, typically evaluated in the strictly controlled setting of randomized controlled trials with close attention to internal validity, safety, efficacy and manufacturing - HTA bodies have different remits and, therefore, additional evidence requirements. Criteria for reimbursement decisions vary across countries but can include unmet medical needs, the relative effectiveness and safety of the drug, drug price, budget impact and cost-effectiveness. Designing a study suitable for regulatory approval might not always translate into data suitable for reimbursement decisions, creating an evidence gap between the regulatory and reimbursement submission and posing a hurdle to patient access to new drugs in some countries. Indeed, even when a marketing authorization is obtained, HTABs and decisions on drug pricing and reimbursement often delay access to medicines for patients at a national or even regionallevel. For the development of new and innovative medicines it is therefore essential that discussion is initiated between industry, EMA as well as reimbursement agencies at an early stage.
Autorenporträt
Ulrike Fuchs, MSc.: Study programme Medical and Pharmaceutical Biotechnology at the University of Applied Sciences Krems. Regulatory Affairs Associate at Shire, Vienna.