Agathe Guillot is the Head of Regulatory Affairs at the Cell and Gene Therapy Catapult. She brings over 13 years’ experience in regulatory sciences with a particular expertise in global clinical and non-clinical regulatory from large pharma and biotech organisations. She also developed her GCP expertise as a MHRA GCP inspector. She is a trained pharmacist and holds a masters degree in European regulatory affairs. Her and her team provide regulatory affairs expertise across all stages of the product development at UK, European and global levels.
