Manufacturers
This webinar will provide an overview of pre-approval information exchange (PIE), review the changes and discuss the implications of the recently released AMCP Format v4.1, and provide manufacturer considerations and recommendations for PIE and the pre-approval dossier.
How are biosimilar manufacturers approaching patients, providers and payers? What can they do to differentiate? Xcenda shares insight from our field programs.
In this digital age, how can pharmaceutical manufacturers leverage innovative tools to prove their product's value proposition and overcome market access challenges?
An executive Q&A on challenges and opportunities related to reimbursement, coding and coverage for cell and gene therapies.
An executive Q&A on the role of data and the future of innovative reimbursement modeling for cell and gene therapies.
Xcenda examines the impact of the ICER value assessment framework on payer perceptions.