SFL’s Head of Combination Products Theresa Jeary will present as part of a training course on the New Medical Device Regulation at the Management Forum (London, 24-25 September 2019). Theresa’s presentation will address the impact of the incoming MDR on conformity assessment and medical device manufacturers and distributors, with a particular focus on the successful implementation of new changes in the areas of clinical development and safety monitoring.

Theresa is an expert in medical devices & combination products and was previously Head of a Notified Body for Medical Devices. Theresa is part of SFL’s vastly experienced Medical Devices and Combination Products Team, providing complete lifecycle support, from strategic advice on development to clinical evaluation, QMS, CE-marking and post-marketing maintenance. Please contact us to find out how Theresa and SFL can support your products.