Sally Sennitt

Sally Sennitt MBBS, FRCA is currently the medical affairs director at RQM+ focusing on clinical aspects of pre-market MDR CE submissions, post-market studies and data collection. She has 10 years experience in medical device consulting to which she brings a pragmatic and creative approach based on her previous international experience in both clinical medicine and the devices industry.

She completed medical training in London and specialised in anaesthesia. Clinical work took her to Switzerland and South Africa as well as the UK after which she cofounded a Belgian medical device start up, setting up the quality, regulatory and medical affairs functions from scratch and gaining CE Marks and 510k clearances for the product portfolio. After an 8 year stint heading up the central laboratory of the largest stem cell bank in Europe, she returned to the world of medical devices in regulatory consulting.

She is well versed in developing clinical strategies, writing and reviewing CERs, designing post-market clinical investigations, navigating Notified Body reviews and is currently studying for an MSc in Regulatory Affairs at Trinity College Dublin to maintain an edge in terms of current knowledge and critical application.