We are very pleased to welcome Signe Hanghøj to the MedicQuant ApS team this May.

Signe has joined us as Quality Assurance and Regulatory Affairs Director, bringing extensive experience in building quality management systems in the MedTech industry. Her strong background in developing and achieving QMS certification will play a key role in establishing a robust quality culture at MedicQuant - paving the way for our point-of-care IVD product to reach the market.

"I'm excited to join MedicQuant and contribute to its mission-driven team. I aim to apply my 10 years of experience in the medical device industry by building a QMS that is fit for purpose and positions MedicQuant for regulatory approval and market entry. This means establishing the technical documentation, processes, and quality infrastructure the company needs to bring its product to patients safely and compliantly. I look forward to working together with the team at MedicQuant to make all of this come true." says Signe.