January 15, 2025 C-Path Welcomes Bayer Pharma as Newest Member of CPP C-Path is excited to welcome Bayer Pharma as a the newest member of the organization's Critical Path for Parkinson’s (CPP) Conso
C-Path’s TRxA Announces 2025 Request for Proposals from Academic Investigators New Funding Opportunity for Drug Development Projects TUCSON, Ariz., January 14, 2025 – Critical Path Institute’s® (C-Path) T
January 12, 2025 National Pharmacist Day: Recognizing These Pillars in Healthcare Every year on January 12th, we pause to celebrate National Pharmacist Day — a day dedicated to recognizing the vital role pharma
January 28, 2025 TRxA Funding Opportunities 2025 Join us on January 28th at 10am EST as C-Path’s Translational Therapeutics Accelerator...
December 13, 2024 Real-world evidence in the cloud: Tutorial on developing an end-to-end data and analytics pipeline using Amazon Web Services resources In the rapidly evolving landscape of healthcare and drug development, the ability to efficiently collect...
December 12, 2024 The Power of Data Sharing and Collaboration Across LGMDs in a Pre-competitive, Neutral Environment This event featured Dr. Volker Straub, a renowned neuromuscular genetics expert...
November 27, 2024 Voice of the Patient report Externally-Led Patient-Focused Drug Development (EL-PFDD) Meeting for ARPKD Patients and their Families Autosomal Recessive Polycystic Kidney Disease (ARPKD) is a rare genetic disease. It occurs in about one in 20,000 births...
November 27, 2024 Autosomal Recessive Polycystic Kidney Disease (ARPKD)Adjunct EL-PFDD Scientific Workshop Report The mission of the Polycystic Kidney Disease Foundation is to fund research, advocate for patients, and ultimately to end PKD..
December 10, 2024 Biomarkers 101: A Patient’s Perspective on the Importance of Identifying New Biomarkers Biomarkers are emerging as powerful tools in the field of kidney health, playing a crucial role in the diagnosis, monitoring...
November 27, 2024 A computational tool to optimize clinical trial parameter selection in Duchenne muscular dystrophy: A practical guide and case studies Duchenne muscular dystrophy (DMD), a rare pediatric disease, presents numerous challenges when designing clinical trials...