Theresa JearyHead | Birmingham, England
Theresa Jeary joins the Lloyd’s Register Quality Assurance (LRQA) Medical Directives team as Technical Manager with responsibility for device/drug combination products. Theresa also has experience of the CE certification and Clinical expertise of medical devices used for assisted reproduction techniques, organ transplantation procedures, vascular, wound care and devices utilising animal tissue, as well as having a background in the development and commercialisation of Pharmaceutical and medical device products.
She joins from BSI where she was their combination product expert for five years, managing the consultation process for Devices containing ancillary medical substances or ancillary blood derivatives. She is well known within the Device/Drug product arena and is regularly asked to speak at European conferences about the regulatory requirements.