Brix Bayuga is a seasoned Global Regulatory Affairs and CMC (Chemistry, Manufacturing, and Controls) expert with over 16 years of experience in the pharmaceutical industry. As Senior Manager of Global Regulatory Affairs at Pfizer, where he has dedicated more than 13 years, Brix has a proven track record in navigating the complexities of regulatory landscapes across the US, Europe, ASEAN, China, and Japan. He specializes in developing and executing robust regulatory strategies, managing new submissions, lifecycle management, and liaising with Health Authorities worldwide. Brix’s deep expertise extends to hands-on operational experience at manufacturing sites, ensuring compliance and quality assurance at every stage. His strategic insights and comprehensive knowledge make him a key contributor to high-impact regulatory projects, particularly in oncology and quality assurance management.

At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the discovery, development and manufacture of health care products, including innovative medicines and vaccines. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time. Consistent with our responsibility as one of the world's premier innovative biopharmaceutical companies, we collaborate with health care providers, governments and local communities to support and expand access to reliable, affordable health care around the world. For more than 170 years, we have worked to make a difference for all who rely on us.