Afrah Mujeeb

Afrah Mujeeb is a Regulatory Affairs professional with expertise in regulatory compliance, quality assurance, and emerging technologies in the pharmaceutical and medical device industries. She is currently pursuing her Master of Science in Regulatory Affairs at Northeastern University, where she focuses on regulatory strategy, AI-driven compliance, and medical device regulations.With hands-on experience in regulatory intelligence, FDA submissions, and quality management systems (QMS), Afrah has worked on projects involving AI/ML applications in regulatory decision-making. She has contributed to FDA draft guidance reviews and actively engages with industry organizations such as ISPE and RAPS.Afrah’s passion lies in bridging the gap between technological advancements and regulatory frameworks, ensuring AI-driven innovations align with global compliance requirements. She is dedicated to fostering industry discussions on AI transparency, validation strategies, and regulatory harmonization efforts.