Anneli Wiedenkeller
Senior Quality and Regulatory Consultant

Anneli has worked within the medical device industry since 1988 and the recent years as a senior product assessor at one of the largest Notified Bodies worldwide.
Her experience includes several areas such as regulatory affairs, quality assurance, product development, education, manufacturing and service, with focus on electro medical devices. She is an excellent communicator, focused and goal oriented and has a long experience of both team work and individual tasks. She is a skilled and appreciated trainer of  our MDR courses.

“Why all these tiring requirements of documentation everywhere?”
”An early awareness and documented implementation of the regulatory requirements does not only help you to fulfill the legal safety and performance aspects for market access, but also force you to regularly assess your current results for maintaining a product and an organization in the state of control.”