“We are very happy to welcome Peter Fröberg to RegSmart as Director, Medical Device. Peter has a long and broad experience from the global medical device sector working with the complete product life-cycle, never losing sight of the market. Peter is a solution-oriented person with a strong record from strategic regulatory decision-making roles and he perfectly matches our motto “fit-for purpose”. Peter will be responsible for building RegSmart’s medical device service, offering strategic and regulatory advice to the clients. A warm welcome Peter”, says Marie Gårdmark, CEO, RegSmart LifeScience.
With 20 years of experience within the medical device sector, I am immensely proud to get this opportunity to support medtech companies with their strategic and regulatory challenges. Finding solid and pragmatic solutions and to convey knowledge, enabling a smooth transition into the changing regulatory landscape. All with the aim to shorten time to market.
I have extensive experience in driving and developing a product area within medtech, working with the complete product lifecycle in mind. Planning and prioritization within the regulatory strategies, working with applications and authorities, supporting in developing clinical proof and to navigate during times of a changing regulatory landscape, have provided me with a broad and deep knowledge in the field. These experiences together with a background in engineering and product development, and many years as product manager building strong, trustful relations have helped me to solve many strategic and regulatory obstacles along the way.
To put it short; A person who finds joy in the process of creation, solving problems and conveying knowledge amongst dedicated and talented people!