Boyds
Celine Courtay-Cahen has extensive experience in regulatory affairs, with a focus on gene therapy, orphan drug applications, and interactions with FDA and EMA. Celine has worked in various roles such as Senior Regulatory Affairs Manager, Regulatory Affairs Executive, and Project Manager. Celine's background includes research in canine cancers and breast cancer cell lines, as well as post-doctoral work on the cytoskeleton during the cell-cycle. Celine holds a PhD in Molecular Biology and Genomics, along with a Master's in Biochemistry.
Boyds
At Boyds, our goal is to facilitate the translation of cutting-edge science into medicinal products which benefit patients. We understand how challenging this can be, both technically and commercially. Our service is designed to provide crucial experience and assistance whenever you need it, in order to bring your innovations to the marketplace as quickly and efficiently as possible. Boyds was established in 2005 and provides a range of expertise and skills central to the development of pharmaceutical and biotechnology medicinal products and medical devices. We are headquartered in the UK with offices located in Cheshire and Cambridgeshire and also have offices in Dublin and Pennsylvania. Our consultancy services offer a cost-effective solution for those requiring expert assistance in order to expedite development, add value to their product, and reach those key milestones. Whether it relates to a single issue or a long-term commitment to your development team, we can help you chart the innovative course great science demands.