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Streamline the lifecycle of critical documents with a secure, compliant, and collaborative platform designed to simplify approvals, ensure traceability, and maintain regulatory readiness.
In highly regulated sectors like pharmaceuticals, biotechnology, and medical devices, managing documents isn’t just about organization—it’s about maintaining compliance, ensuring traceability, and enabling process efficiency. ACE Docs is purpose-built to address these industry challenges, empowering your teams to stay audit-ready and compliant while streamlining critical workflows.
Enable real-time collaboration with Office 365 integration, perfect for authoring SOPs, protocols, and regulatory submissions. ACE ensures your documents remain compliant with industry standards like FDA 21 CFR Part 11 and ISO 13485.
Tailored access controls ensure only authorized personnel can view, edit, or approve sensitive files, a necessity for managing controlled documents like batch records or validation protocols.
Maintain full traceability with automatic version histories, approval timestamps, and access logs, making audits and inspections seamless.
ACE simplifies the complex regulatory landscape, making it easier for your organization to meet global standards. Whether it’s managing CAPA documentation or ensuring training records are accessible and accurate, ACE is your trusted partner in compliance.
ACE comes with workflows tailored for change control, deviation management, and nonconformance reporting, reducing manual errors and ensuring regulatory alignment.
Accelerate approvals with compliant, secure e-signature functionality, helping you meet the demands of electronic submissions and regulatory reviews.
Reduce implementation time with pre-validated templates that align with your industry’s best practices, ensuring compliance from day one.
Life sciences organizations require efficiency without compromising quality. ACE Docs delivers real-time insights and collaboration tools to ensure every process—from R&D to manufacturing—is optimized for success.
Keep all critical records, from SOPs to audit trails, in a secure, cloud-based location accessible to global teams, ensuring consistency and compliance.
Facilitate faster decision-making with tools that allow teams to comment, share, and track changes, bridging the gap between R&D, QA, and regulatory teams.
Use ACE Analytics and its reporting features to monitor document workflows, identify bottlenecks, and ensure processes like product launches and inspections stay on track.
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Maximize the value of your document management with ACE®.
