Andrea Sisneros PhD

Andrea Sisneros has 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 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.