has been working as a lawyer specialising in medical law since April 2016. Since 2017, she has been advising pharmaceutical companies and manufacturers of medical devices at Sträter Rechtsanwälte on the following key areas: Questions of clinical trials of medicinal products and medical devices; Contractual design in the conduct of clinical trials and non-interventional studies; Legal framework conditions with regard to research funding of medical institutions; Regulatory and general questions in the area of national and European authorisation and conformity assessment procedures; Legal aspects of data processing in the healthcare sector.