Advocacy and Legal Update 340B Reform Bill Introduced in House by Johanna Gray, Artemis Policy Group In late May, Reps. Bucshon (R-IL), Carter (R-GA), and Harshbarger (R-TN) introduced the 340B Read the full article…
Member and Community Relations Update Genetic Testing Program Launched by Hemophilia Alliance by Angie Blue, Director of Member and Community Relations The Hemophilia Alliance is excited to announce a new Read the full article…
Administration and Operations Update Welcome to Our New Online Home! by Administration & Operations Team After months of dedication and hard work from our team, we are thrilled to finally Read the full article…
Notes From The Community Do you have a passion for sharing your knowledge and experience in hemophilia care and management? The Hemophilia Federation of America is excited to invite speakers Read the full article…
In this Issue… Jeff Weighs In Administration and Operations Team Update · Don’t Miss Out! Navigating Patient Assistance and Copay Assistance Schemes Webinar · Re-cap of the 1st Annual Hemophilia Read the full article…
Jeff Weighs In by Jeff Blake, President and CEO Also in this Issue… Administration and Operations Team Update · Don’t Miss Out! Navigating Patient Assistance and Copay Assistance Schemes Webinar Read the full article…
Administration and Operations Team Update Don’t Miss Out! Navigating Patient Assistance and Copay Assistance Schemes Webinar The Hemophilia Alliance will be presenting a special webinar on understanding the difference between Read the full article…
Advocacy and Legal Update New Research on 340B Program Spending Highlights Differences Among Covered Entities by Elizabeth ‘Issie’ Karan, Legal Counsel In a presentation at the 13th Annual Conference of Read the full article…
Member and Community Relations Team Update MCR’s In the Community – MCR Team The Member and Community Relations (MCR) Team is comprised of Angela Blue, Jeff Amond, Karen Bowe-Hause, Read the full article…
Notes from the Community VWD Connect Foundation Annual Conference in July: REGISTRATION STILL AVAILABLE! VWD Connect Foundation (VCF) will be holding the 8th Annual National Type 3/Severe Von Willebrand Disease Read the full article…
