• Topics

  • Formats

Organiser: DIA

Despite broad recognition of the value of patient, care partner, and advocacy input in research, engagement often occurs late or without a clear connection to early scientific and development decisions.

This white paper reflects a collaborative effort between BMS teams and patient advocacy leaders, who co-authored the work, to define what early engagement looks like in practice and how it can be applied in routine development.

Reading this content is completely free

Enjoy Unlimited Access and Unlock
Additional Features with a Free Account

Join Now

You are attempting to log out of MyMA

Do you really want to log out?