11 Jul 2022 | 02:45 PM GMT
Past Meeting

Oncology Digital Health: Evidence Requirements from Payers and Regulatory Bodies

About this Meeting

The marriage of digital health and oncology is very new, with companies still figuring out the best approach to establish in the market. For entrepreneurs, it is important to have as many options as possible, which makes clinical and economic evidence critical for most solutions to ease adoption. This requires a nuanced understanding of what the evidence standards are for different stakeholders. In this meeting, we will focus on payers and regulatory bodies.  

Join this session to break down the key questions:  

  • How can companies build an evidence base that is robust but also flexible enough to satisfy both payers and regulators in a cost effective manner?  
  • Working with payers has been an early area of opportunity within digital health and oncology, but many require clinical trials. Is this a good route for young companies?   
  • The nature of cancer treatment means that digital health is unlikely to treat the underlying issue. Digital products can play many roles within treatment - such as supporting mental health, comorbidities, etc - so how can companies build an evidence base that demonstrates both efficacy and value?  
  • What health economics results do digital health companies need to show to convince payers? Most payers look at health economics data and get interested when healthcare costs reduce. What are their expectations from digital health solutions in oncology?  
  • Due to the lack of industry-wide evidence frameworks for digital health, payers and regulators requirements are usually the same as drugs or medical devices. However, digital health solutions are very different in nature. How can the industry work together to evolve the evidence requirements from payers and regulatory bodies?

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