All the answers to your questions.

The Confideck Initiative is a European-driven effort uniting high-tech innovation with deep regulatory expertise to simplify compliance for the medical device and in-vitro diagnostic industries. Our mission is to empower manufacturers with advanced, reliable solutions that accelerate certification and support innovation.

Confideck’s platform is designed for medical device and in-vitro diagnostic manufacturers to simplify technical documentation. Combining enterprise-grade compliance, seamless MS Office integration, and user-friendly automation, Confideck streamlines regulatory processes for faster and more reliable outcomes.

Confideck’s automation tools eliminate repetitive tasks, minimize errors, and accelerate (re)certification processes. By automating critical steps, Confideck frees your team to focus on driving innovation and meeting core business goals.

Our servers are located exclusively within the European Union (Germany), compliant with GDPR and other relevant data protection regulations. The infrastructure is certified to ISO 27001, ISO 27017, ISO 27018, and ISO 9001 standards. Confideck prioritizes data security and operational integrity.

Confideck caters to companies of all sizes, from global enterprises to growing startups. Built on adaptable configurations, our platform scales to meet your unique needs while delivering value across industries.

Confideck software is fully verified to meet stringent quality and compliance standards. Our team is available to assist with your validation efforts, ensuring seamless integration into your processes.