Cure HHT
Review and Comment on Material Transfer Agreement
There are no treatments or cures for HHT - the second most common inherited...
Lawyers, we need you! Volunteer to support the rare disease community.
Volunteer hereRare disease is anything but rare. As many as 7,000 rare diseases affect 300 million people globally. Yet worldwide, patients are meeting these challenges head-on. Rare disease research often involves navigating complex regulatory landscapes. Lawyers are needed to ensure compliance with all relevant regulations and laws governing research, clinical trials, and the eventual dissemination of treatments.
WTA lawyers are working closely with patient-led organizations in the Rare As One Network. Partners include: