Regulatory Affairs and Compliance

The Regulatory Affairs and Compliance team at SI-BONE Inc. is responsible for ensuring that the company's medical devices meet all regulatory requirements and compliance standards throughout their development and commercialization. This team collaborates closely with medical, clinical, and market access functions to facilitate the approval process for the iFuse Implant System, ensuring it complies with FDA and international regulations while maintaining high safety and efficacy standards for patients with sacroiliac joint disorders.