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Audrey Toulemonde, MSc (she/her/hers)

Associate Director, Medtech Services
Cencora, United Kingdom

Audrey Toulemonde is an Associate Director at Cencora.
With 15 years of experience in regulatory affairs, she has covered all aspects of medical devices and drug-device combinations lifecycles, from product development to preparing technical documentation and overseeing lifecycle management in Europe and the UK. Audrey is skilled in conducting literature reviews and writing clinical evaluations across a range of medical device technologies. Her expertise also includes clinical trial applications for medicinal products, marketing authorization processes, and ongoing life-cycle maintenance. In recent years, she has expanded her understanding of MD/IVD regulations, especially as they pertain to medicinal clinical trials using MD/IVDs and combined studies.

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