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What's your Rare Disease Summit Game Plan?

What’s your main goal for attending the Rare Disease Summit?

A. To stay ahead of industry trends and hear from top experts.

B. To network with pharma, biotech, and advocacy groups.

C. To learn about the latest innovations in rare disease treatments.

D. To advocate for better patient access and engagement strategies.

Your ideal networking conversation would be with…

A. A CEO or regulatory expert discussing the future of rare disease therapy.

B. A patient advocacy leader or nonprofit founder sharing their impact stories.

C. A biotech innovator revealing breakthroughs in gene therapy and AI.

D. A payer or policymaker discussing the healthcare access landscape.

What’s your biggest challenge in rare disease innovation?

A. Understanding the regulatory and commercialization pathway.

B. Building strong collaborations between pharma, advocacy, and research.

C. Navigating scientific advancements and emerging technologies.

D. Overcoming barriers to pricing, reimbursement, and patient access.

How do you prefer to learn?

A. Keynote talks from industry leaders and regulatory experts.

B. Interactive roundtable discussions where I can share and exchange ideas.

C. Scientific deep dives on cutting-edge research and therapies.

D. Case studies and panel discussions on real-world patient impact.

If you could leave the summit with one key takeaway, what would it be?

A. A clearer understanding of regulatory and policy shifts in rare disease.

B. A stronger network of partners in pharma, advocacy, and research.

C. Inspiration from cutting-edge biotech breakthroughs.

D. Actionable strategies to improve patient access and affordability.

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