From idea to certified medical device: IPP supports MedTech teams with specialized consulting and a ready-to-use ISO 13485- and MDR-compliant QMS. For faster compliance, clear processes, and a more efficient path to market readiness.
IPP helps MedTech teams move faster with expert consulting and scalable systems.
ipp. Dr. Klügl supports MedTech start-ups and companies with specialized consulting throughout the entire product lifecycle. Areas of focus include Regulatory Affairs, ISO 13485 quality management, MDR compliance, and technical documentation for regulatory submissions. The team also provides project management, process design, and strategic support — from initial concept to market readiness.
The Easy13485 Makerspace is a structured alternative to traditional consulting. It gives MedTech teams a ready-to-use quality management system with templates, training, and audit preparation built in. Start-ups gain a preconfigured, ISO 13485- and MDR-compliant process framework that helps them reach compliance and certification faster and with greater independence.
