Senior Regulatory Consultant, IVD
Namsa, France
With over five years of regulatory experience in the medical device industry, Christèle East Ph.D works closely with clients to maintain and expand their marketing authorisations in the European Union. She has worked in the Biotech/Pharmaceutical industry for over 20 years, including 10 years in IVD product development, primarily in the fields of immuno-oncology and virology. Christèle started her career in R&D, working in all phases of development, then moved to a QC position, obtained a University degree in clinical research, before finally specialised in regulatory affairs to develop broad regulatory experience in the field of MD and IVDs.
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Recent developments in UK regulations for IVDs: implications for EU manufacturers.
Thursday, May 11, 2023
11:45 – 12:45 CEST