Speaker details

Biography

JOSEFINE SOMMER is an experienced EU regulatory and compliance lawyer, advising pharma, biotech, and medical device clients on complex aspects of product life cycle management under EU law. Josefine also advises investors in relation to the regulatory due diligence for transactions. As a Medical Devices Quality Systems Lead Auditor, she supports clients in inspection and audit matters as well. Josefine advises the life sciences industry, covering pharmaceuticals and biotech, medical devices and IVDs, digital health and combination products, as well as cosmetic food.