Caroline Ehrenborg
Quality and Regulatory Consultant

Caroline has many years of experience with medical devices (combination device/drug), both from a regulatory and a research & development perspective. She has worked with global product registrations, quality assurance, design control and product development. 

With her background, including MDR preparations, Caroline helps clients to focus on the right issues and avoid pitfalls during design & development work, to get a smooth regulatory approval.

Caroline loves new challenges and is eager to understand the benefit of each medical device. She has an eye for details, is very structured and delivers effectively in a timely manner.  She has excellent communication skills and creates technical documents with a logical structure.

Caroline holds a MSc in Biotechnology from the University of Linköping.