Rebeca Rapozo is a pharmacist and medical device consultant with a strong background in regulatory affairs and medical affairs. She holds postgraduate qualifications in project management and toxicology and is currently pursuing a master’s degree in microbiology and immunology. Over the course of her career, she has worked with medical devices, pharmaceuticals, and biologics, supporting companies in navigating complex regulatory landscapes and developing robust compliance strategies.
In addition to her consulting work, Rebeca is a trained clinical laboratory technician and has hands-on experience within silico testing, an area in which she has also published. Her multidisciplinary expertise – spanning clinical research, toxicological evaluation, and regulatory science—positions her to bridge technical, scientific, and business perspectives in the healthcare sector.