AGATHE GUILLOT

Head of Regulatory Affairs, Cell and Gene Therapy Catapult

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.

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