Regulatory Affairs and Compliance

The Regulatory Affairs and Compliance team at Travere Therapeutics is responsible for ensuring that the company adheres to all regulatory requirements and quality standards in the development of therapies for rare diseases. This team plays a critical role in the preparation and submission of regulatory documentation, maintaining compliance with Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP), and managing risk to ensure that products are safe and effective for patients. Their efforts support the overall mission by facilitating seamless communication with regulatory agencies and maintaining high-quality standards throughout the product lifecycle.