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Elevate compliance oversight with a robust audit management solution that simplifies planning, execution, and reporting while driving continuous improvement across your organization.
Audits are a cornerstone of compliance in life sciences, ensuring adherence to regulations like FDA 21 CFR Part 11, ISO 9001, and EU GMP. ACE’s Audit Management simplifies the planning process, allowing your organization to focus on quality improvement rather than administrative hurdles.
Plan and manage internal, supplier, and regulatory audits with a single, unified calendar that assigns tasks, sets deadlines, and tracks progress.
Use pre-configured audit management process workflows tailored for life sciences audits, reducing preparation time and ensuring all required elements are covered.
Keep stakeholders informed with automated notifications about upcoming audits, tasks, and post-audit activities.
In a highly regulated environment, capturing audit findings accurately is critical. ACE enables seamless, real-time documentation of audit activities, whether performed on-site or remotely.
Leverage configurable checklists to ensure every audit covers the necessary scope, from supplier qualification to GMP compliance.
Attach photos, documents, and notes directly to findings, ensuring all evidence is securely stored and traceable.
Conduct remote audits with integrated tools that enable real-time collaboration between auditors and auditees.
The value of an audit lies in the actions taken to address findings. ACE ensures that audit outcomes lead to meaningful improvements by integrating with corrective and preventive action (CAPA) workflows.
Prioritize findings based on risk, enabling your team to focus on the most critical issues first.
Automatically generate CAPA records for significant findings, ensuring timely resolution and compliance tracking.
Generate detailed audit reports and dashboards to identify trends, track progress, and demonstrate compliance during inspections.
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Maximize the value of your audit management with ACE®.
