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Director at Riodove, UK
Andrea Sisneros has 16 years’ experience in Regulatory Affairs project management in both the CRO and Pharma environments. She has 4 years’ clinical trials experience with applications to both competent authority and ethics submissions along with a working knowledge of the varied marketing authorisation application routes. Andrea’s experience also encompasses CMC work of 6 years arising from acquisition of various divested product types and through change of ownership. She has managed a wide product portfolio which includes investigational medicinal products and OTCs comprising medical devices and medicines.