CogniDox
A lean, scalable eQMS platform for medical device and high-tech product development
About CogniDox
CogniDox is a flexible electronic Quality Management System (eQMS) designed to streamline document control, design processes, and regulatory compliance for medical devices, biotech, pharma, and high-tech industries. With features like FDA 21 CFR Part 11 compliant e-signatures, CAPA management, and integrated learning management, CogniDox helps teams achieve audit readiness while accelerating innovation. Built for scalability, it supports businesses from startups to large enterprises, offering configurable workflows and real-time technical documentation assembly.
FAQ
You can access expert help and product documentation through the Cognidox Support page. For fast, flexible help, try Cognito, their online customer assistant. If you need to raise a support ticket, email the Cognidox Support Team at support@cognidox.com.
Yes, Cognidox supports FDA, MHRA, and ISO standards. It also offers integrated FDA and ISO 13485 compliant e-signatures for your eQMS.
Cognidox serves industries such as Medical Devices, Biotech & Pharma, CROs & CMOs, High Tech Products, and Consultants.
Yes, Cognidox offers a free trial. You can find more details on their website under the Free Trial section.
Customers can log in to their Cognidox account to download product updates, release notes, and documentation.
Cognidox offers an integrated Learning Management System (LMS) for training, assessments, and streamlined onboarding.
Cognidox provides support for GxP and FDA software validation requirements.
Cognidox offers change control features to manage changes when it matters most, ensuring oversight and control with graphical business management tools.
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