The Confideck Initiative is a European initiative that combines high-tech innovations with in-depth regulatory expertise to simplify regulatory compliance for the pharmaceutical, medical device and in vitro diagnostics industries. Our mission is to provide manufacturers with advanced, reliable solutions that reduce manual, redundant tasks and ensure compliance.

The Confideck platform was developed specifically for manufacturers of pharmaceuticals, medical devices and in vitro diagnostics to simplify the creation of technical documentation. By combining compliance control, seamless MS Office compatibility and user-friendly automation, Confideck accelerates regulatory processes and ensures reliable results.

Confideck automates recurring tasks in technical documentation, reduces manual intervention and increases efficiency. This leaves more time for innovation and quality assurance. This makes it easier to create, update and content consistency.

Our servers are located exclusively within the European Union (Germany) and comply with the GDPR and other relevant data protection regulations. The underlying infrastructure is ISO 27001, ISO 27017, ISO 27018 and ISO9001 Certified. Confideck places the highest value on data security, availability and operational integrity.

Confideck was developed specifically for regulated companies in the life science industry — in particular for manufacturers of medical devices and in vitro diagnostics. The platform is suitable for organizations of all sizes who want to make technical documentation more efficient, secure and sustainable. Thanks to the flexible architecture, the Microsoft-compatible environment and integration into existing systems, Confideck adapts to your structures — not the other way around.

The Confideck software is fully verified and meets the highest quality and compliance standards. Our team helps you with validation and ensures seamless integration into your existing processes.