Clinical and Regulatory Affairs

The Clinical and Regulatory Affairs team at Zevra Therapeutics is dedicated to ensuring the successful development and approval of innovative therapies for rare diseases. They manage clinical trials, navigate complex regulatory landscapes, and collaborate closely with key stakeholders, including thought leaders and advocacy groups, to address unmet patient needs. By employing creative solutions and maintaining a focus on data-driven decisions, the team facilitates the timely progression of life-changing therapeutics from concept to market.