Regulatory compliance of medical devices (including software) made simple
Do you find regulatory compliance confusing? We can make it easy.
Join us for a two-hour best-practice session talk with LU Innovation to learn more about the opportunity to simplify regulatory processes (such as ISO9001/13485 & CE-mark). Get a better understanding of how to overcome regulatory obstacles, and speed up innovations to improve healthcare.
Through our partnership with MyBlueLabel, a Danish regulatory consultant, LU Innovation can help make the process:
Simpler: through pre-set templates to help you gain market access (MDR/FDA etc.)
Faster: digitalized processes help fast-track regulatory compliance.
More transparent: get clear information, fixed times and costs upfront.
Don't miss the opportunity to enhance your understanding and speed up the regulatory processes for your potential medical device products.
Limited seats. Reserve your spot!