Patient Advocacy

How Advocacy Perspectives Can Improve Neurology Research

July 13, 2026

Inclusive Research Starts Locally: Improving Trial Readiness Through Community‑Based Models

April 23, 2026
Life Science Podcast

Rare Disease Day Insight: Epilepsy Care Gaps in Pregnancy with UCB’s Andrea Wilkinson — Episode 244

Improve Recruitment Outcomes Through More Diverse Clinical Trials

April 09, 2026

When patients lead: Breaking barriers in ultra-rare disease drug development

March 03, 2026

Site Selection Solutions Using Patient Insights for Rare Disease Trials

February 20, 2026

The Critical Need to Address Mental Health in the Rare Disease Community

December 11, 2025

Patient Recruitment Strategies: Empowering Patients Through Accessible Information

October 01, 2025
Biotech Blogs

Embedding the Patient’s Voice in Drug Development

Advancing the Next Parkinson’s Disease Breakthrough: Keys to Successful Clinical Trials

September 16, 2025
Life Science Podcast

Championing the Patient Voice with Ardelyx’s Chief Patient Officer Dr. Laura Williams — Episode 216

Patients First: Revolutionizing Patient Recruitment in a Dynamic Landscape

June 04, 2025
Biotech Blogs

Creating Inclusive Clinical Trials: Why Authenticity and Patient Stories Are Essential
Life Science Podcast

Bridging Science and Advocacy with Lawreen Asuncion, Life Science Professional and Rare Disease Patient Advocate
Life Science Podcast

FNIH’s Dr. Travaglia and ALS Patient Advocate Dr. Sethi Discuss New ALS Program
Blogs

The National Kidney Foundation’s Role in Advancing Clinical Trials in Nephrology