For researchers who want to accelerate innovations in the medical technology field with the aim of improving healthcare, it is necessary to follow and apply the regulations for medical technology products. To facilitate and make it easier for researchers to comply with the regulations to achieve ISO9001/13485 requirements and CE marking, LU Innovation is organizing a seminar on how the time to approved product can be shortened while reducing costs.
"Many find the regulations for medical technology products time-consuming, expensive, and complicated. Through a partnership with a Danish regulatory consultant, MyBlueLable, this process can be made faster, cheaper, and with increased transparency", says innovation developer Cecilia Jädert at LU Innovation.