Lukas Losigkeit has been active in the medical device sector since 2016 and is Managing Director of thinqbetter GmbH since 2019.
His core competencies include quality management systems and regulatory approvals for medical devices and in vitro diagnostic medical devices (IVDs). He has gained extensive experience in clinical affairs, regulatory affairs, and design control, which he now shares in training sessions.
As a trainer at the qtec Academy, he teaches topics such as clinical evaluation, risk management, performance evaluation, and technical documentation.
What matters most to him as a speaker: "Many challenges in market approval arise from a lack of experience with ever-evolving regulatory requirements. In my seminars, I aim to create clarity, alleviate concerns, and empower participants to handle complex topics independently and successfully."