Author name: Claritas Rx

Commercializing a therapy for rare diseases is a challenging endeavor. With the complexities of patient access, regulatory hurdles, and stakeholder engagement, manufacturers must adopt a carefully crafted strategic framework. In a recent Access USA panel discussion, industry experts shared their valuable perspectives on this topic. The panel featured Justin Bush from Pharavis, Richard Wilson from

Specialty pharmacies (SPs) play a crucial role in delivering complex medications to patients who require ongoing support throughout their treatment journeys. However, the effectiveness of SPs often hinges on timely intervention, efficiency, and seamless collaboration among stakeholders. These challenges are further amplified by time-consuming manual processes, delayed responses, and lack of real-time visibility into patient

Guiding patients through their treatment journey is a critical yet intricate task for patient services teams. One of the biggest obstacles they face is “patient drop-off,” the moments when individuals disengage or discontinue treatment. These drop-offs can significantly impact healthcare outcomes, operational efficiency, and access to care. This blog explores the key stages in the

Macular telangiectasia (MacTel) type 2, a rare neurodegenerative eye condition, has long left many without access to effective treatment. This disease silently affects central vision, making everyday tasks like reading and recognizing faces increasingly challenging for those impacted. However, patients and biopharma professionals alike have reason to look ahead with renewed optimism. On March 6,

Every year, millions of people around the world come together to show support and amplify the voices of those living with rare diseases. Rare Disease Day, observed on February 28 (or 29th on leap years), is a vital opportunity to increase public awareness and understanding of rare diseases, their impact, and the need for more