Secure FDA and GXP compliance without slowing down your product roadmap with a single cloud QMS platform. Tap into AODocs’ unique combination of powerful document control, a flexible workflow engine, trusted AI assistants, and full traceability
Ensure speedy regulatory compliance with HIPAA, FDA, and ISO guidelines. Lead on industry standards such as FDA 21 CFR Part 11, ISO 13485, GxP, EU MDR, ISO 14971, and more. AODocs’ QMS offers a turnkey-qualified platform and a validated library.
Control your SOPs, such as work instructions and other critical documents, to ensure consistency, quality, and compliance across your organization. Automate document assembly from preapproved templates and control your content lifecycle, from draft to distribution and end-of-life, with full traceability.
Ensure consistency, efficiency, and quality throughout your organization with a full-feature QMS offering document control, CAPA, audit, supplier and equipment management, and more. Benefit from a versatile platform that lets you easily adapt your processes to your specific needs and effortlessly configure additional document workflows. Automate document assembly using validated templates and manage your content lifecycle from draft to distribution and end-of-life, ensuring full traceability.
Prevent disruptions to operations by ensuring that updated technical procedures, new equipment, facility changes, or recently introduced standards are implemented quickly, controlled, and coordinated. With an integrated change control process, gain full oversight to plan, approve, and distribute procedures, protocols, and other key documentation.
Use AI-powered features to research and design effective action plans to address CAPA and audit findings. Evaluate recommendations made by our system through correlations between newly reported issues and your data to define pertinent strategies and solutions.
Centralize and organize your research manuscripts and lab notes, leveraging generative AI for document classification and analysis. Accelerate FDA submissions by quickly accessing key information hidden in massive unstructured content.
Combine process automation and document management, at scale, while controlling where and how your content is stored
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