Floella Otudeko

Floella Otudeko is a Senior Quality Assurance, Regulatory Affairs, and Human Factors Engineering Consultant with over four years of experience supporting the development and compliance of medical devices and in vitro diagnostics (IVDs). She specialises in MDR and IVDR regulatory strategy, technical documentation, quality assurance, and human factors engineering across the product lifecycle. With a strong interest in medical device software (MDSW), artificial intelligence, and machine learning, she helps manufacturers navigate complex regulatory requirements while developing safe, innovative healthcare technologies.