The Regulatory and Compliance team at XenoPort is responsible for ensuring that all biopharmaceutical development activities align with industry regulations and standards. This team oversees the submission of regulatory documents, manages compliance with health authority guidelines, and collaborates with other departments to facilitate the successful progression of product candidates through clinical development and approval processes. Their expertise is essential in navigating the complex regulatory landscape and safeguarding the integrity of the company’s innovative therapies for neurological disorders.