Liselotte has more than 16 years of experience within the Medical Devices industry.

 

Liselotte spent 11 year within the field of quality assurance and regulatory affairs for IVD devices and Medical Devices at Radiometer Medical Aps.

 

In 2007 Liselotte jointed Coloplast, where she was the Quality Manager for Coloplast Innovation. At Coloplast Liselotte was responsible for CE marking of Class III medical devices.

 

Before joining DMD, Liselotte was Regulatory Affairs Manager at 3Shape A/S.

 

Liselotte is a Lead Auditor for EN ISO 9001 / EN ISO 13485 quality systems and for the Medical Devices Directive (MDD).