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Digital therapeutics: policy, access, value, and evidence


Digital therapeutics are quickly becoming one of the fastest-growing fields in healthcare. Innovation by regulators, policy-makers, and payers is needed to ensure that patients can access and benefit from these technologies.

Successful market access is key to delivering individual patient benefits, potential healthcare system gains, and a meaningful integration of digital therapeutics into our healthcare infrastructure at a population level.

Download this free report, which examines key aspects of policy, access, value, and evidence for digital therapeutics, including:

What are the challenges for reimbursement?
  • What are digital therapeutics and how are they commonly used?
  • The importance of understanding how payers propose to attribute value for digital therapeutics


Pathways for reimbursement across international markets
  • Summarizing some of the key differences in reimbursement pathways
  • Highlighting how some markets are leading the charge, defining and implementing clearer guidelines for the reimbursement of digital therapeutics


Evidence supporting reimbursement of digital therapeutics
  • What evidence is required to achieve optimal reimbursement and market access across markets where paths to reimbursement vary?


US focus: The role of early FDA and payer engagement in access for digital therapeutics
  • Linking regulation, evidence generation, and payer dynamics
  • Looking to the future: the Total Product Lifecycle Program


Asia-Pacific focus: value, evidence, and access
  • How do reimbursement policies for digital therapeutics vary across the Asia-Pacific region?
  • Examining the need for collaboration between technology manufacturers, government, and key local health agencies

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