Michael A. Pereira is a seasoned regulatory and quality executive with over three decades of experience guiding companies through the complex intersection of FDA compliance, global regulatory standards, and business operations. Known for his ability to build and remediate Quality Management Systems across diverse healthcare sectors—including drug, device, biologic, and combination products—Michael has led strategic initiatives for startups and global enterprises alike. With a rare ability to bridge technical and business teams, he brings clarity, structure, and strategic foresight to every challenge, earning a reputation as a trusted leader and advisor in highly regulated industries.

Excited to share my professional biography, highlighting my journey in the medical device industry, my expertise in quality systems and regulatory compliance, and my passion for driving innovation in healthcare technology. With over a decade of experience, I continue to focus on advancing medical devices through strategic quality initiatives and global regulatory alignment.