CAQ.Net – Digitalization from the Shop Floor to the Top Floor
End-to-end software for quality management in the medical technology industry: In this presentation, we will introduce a fully validatable, modular software solution that enables consistent compliance with internal and external requirements as well as regulatory and legal obligations.
Whether it involves implementing medical device-related requirements according to MDR, GxP, FDA, or ICH, or complying with relevant standards and guidelines such as ISO 13485, 21 CFR 820, DIN EN ISO 14971, or 21 CFR Part 11: The CAQ.Net software solution provides comprehensive compliance management that ensures adherence to internal and legal requirements within a well-structured and user-friendly working environment.
Please note: this presentation will be held in German.
Speakers (1)
