OUR SERVICES

Advocacy

Patient association and public affairs engagement.

WHY IT MATTERS

Reimbursement decisions sit inside a wider environment of patients, caregivers and clinicians — people who can describe unmet need and treatment burden in ways a company cannot credibly describe for itself. That only works when the relationships exist before the reimbursement question arrives, when engagement is transparent, and when patient voices stay authentic and independent. We help companies build that engagement early, with appropriate boundaries between industry and patient organizations, and within the Canadian and global codes that govern it.

CAPABILITIES

Patient association mapping

Landscape analysis of Canadian patient groups: priorities, capacity, and relevance to the access questions ahead

Engagement strategies

Structured relationship-building with patient organizations, caregivers and clinicians across the lifecycle

Disease awareness programs

Awareness and education that make disease burden visible before the conversation narrows to a product

Advocacy training

Education that helps patient and other stakeholder organizations understand Canadian approval and reimbursement pathways while preserving their independence and voice

Stakeholder communication

Coherent messaging across patient, clinical and policy audiences, including social channels

Compliance support

Transparent, appropriate boundaries between industry and patient organizations under Canadian and global codes, so legitimate engagement isn't left unexplored

LED BY

Ryan Clarke, LL.B.

Chief Legal & Advocacy Officer | Partner

Let's discuss your advocacy program

Book a call with our team