PRA

The Patient Voice – Engaging Rare Disease Patients to Accelerate Clinical Trial Enrollment

In Advocacy by Freya SmaleLeave a Comment

Rare disease patients face a number of unique challenges and complexities of their conditions, Often, this means that their families and advocates are more engaged with the scientific and research community in comparison to some other disease and patient focus groups. By collaborating with rare disease patients, their families and various stakeholders involved on the design, positioning and subsequent enrollment of clinical trials, studies can be completed faster and more efficiently. PRA Health Sciences’ Scott Schliebner (Vice President, Rare Diseases, Scientific Affairs) and Altair da Silva (Senior Manager, Patient Access and Recruitment Services) are joined by Neil Weisman (Executive Vice President and General Manager at Blue Chip Marketing) to discuss the patient voice and the importance of patient and caregiver insight.

Listen to the podcast here >

Meet PRA Health Sciences at World Orphan Drug Congress USA 2015!

WODC USA

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