With limited data, HTAs have had to make assumptions to inform cost-effectiveness analyses, and companies can suffer if they’re unable to provide evidence-based arguments for their own assumptions, even in rare diseases.
Toronto, Ontario (PRWEB) September 18, 2019
On Wednesday, October 9, 2019 at 11am EDT (4pm BST/UK), join Thomas F. Goss, PharmD, Senior Vice President of Boston Healthcare and Tony Bower, PhD, President of Bower Research Group LLC in a live webinar where they will discuss the challenges of identifying relevant data sources to document disease burden. This is becoming increasingly important for development-stage pharmaceutical and biotechnology companies that are investigating rare diseases.
In this free webinar, attendees will learn about current submission standards for Health Technology Assessments (HTAs). With limited data, HTAs have had to make assumptions to inform cost-effectiveness analyses, and companies can suffer if they’re unable to provide evidence-based arguments for their own assumptions, even in rare diseases.
Topics to be discussed include:
- Assessments of disease burden:
- Disease impact on quality of life
- Costs to the healthcare system
- Evidence to support market access and reimbursement decisions
- Strengths & limitations of available methods of data capture
- Key challenges & potential solutions in identifying relevant data sources
For more information or to register for this event, visit Addressing Evidence Development Requirements for Improved Market Access of Orphan Disease Therapies.
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