Skip to main content

About Us

Company & Expertise

Siotec AG, initially focused on specialised surface technologies, strategically shifted in 2021 to become a CH-REP for medical device manufacturers outside Switzerland and Liechtenstein. Presently, the company offers structured, transparent, and customised solutions for compliant market access in Switzerland and positions itself as a strategic regulatory partner, adeptly navigating manufacturers through the Swiss regulatory landscape with clarity, diligence, and legal precision.

The company's proficiency in the medical technology sector encompasses conducting audits per recognised ISO standards, developing and launching innovative medical devices, establishing and enhancing quality management systems, and structuring the implementation of regulatory projects.

Team

Marc Schmidlin

CEO

Marnie Hückstädt

Quality Management Representative

Marco Granata

Regulatory Affairs Associate

Markus Ramseyer

Person Responsible for Regulatory Compliance (PRRC)