Strengthen compliance and responsiveness in your quality management in the pharmaceutical industry
Between audits, standards, and safety requirements, pharmaceutical quality management requires precision and speed. Yxir helps you centralize your non-conformities, document your corrective actions, and make your critical processes more reliable.
Quality and compliance: pillars at the heart of pharmaceutical challenges
In the pharmaceutical industry, any deviation can compromise batch compliance, impact patient health, or delay market launch.
Quality teams must juggle GMP standards, total traceability, ongoing audits, and just-in-time production requirements. Anticipating non-compliance, ensuring the reliability of CAPA, and tracking every action: these are just some of the challenges that Yxir helps to meet on a daily basis.
A platform designed for the most demanding quality standards
Yxir structures your quality processes from start to finish: anomaly recording, CAPA action plans, documentation, audits, and management. Our platform, enhanced with an AI agent, helps you go faster, further, and safer.
GMP compliance and rigorous documentation
Comply with regulatory and documentation requirements: every quality action is tracked, each batch is associated with its non-conformities and CAPA, all of which can be exported for your audits.
Rapid analysis of quality anomalies
Yxir helps you detect, categorize, and analyze deviations using AI trained on real-world cases. You save time on analysis and decision-making.
Seamless tracking of CAPAs and corrective actions
From reporting to closure: each CAPA is managed, assigned, commented on, and tracked with precision. No more action plans left stuck in an Excel file.
Simplified preparation for inspections and audits
Centralize all your quality data and generate clear, structured reports that meet the expectations of health authorities.
Yxir, the quality ally of demanding teams in the pharmaceutical industry
Deviation detection, CAPA management, regulatory compliance: Yxir supports pharmaceutical manufacturers in achieving smoother, more reliable, and more responsive quality.
Your one-stop quality database
Unify your quality and business data to make better decisions
Centralise all your audits, non-conformities, checklists and field visits in a single intelligent platform. Thanks to assisted data entry, each anomaly is structured and can be exploited, whatever the user's level of experience. Your history becomes a knowledge base that can be used to anticipate, analyse and progress.
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Your digital workflow for resolving drift
Solve faster, thanks to business intelligence
From creation to closure, every stage of drift management is automated and customizable. Intelligent categorization, adaptation of workflows to your internal processes, real-time monitoring... You save time and make anomalies processing more reliable, without ever having to start from scratch.
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Your quality actions implemented without friction
Manage and monitor actions
Plan, assign and track: corrective and preventive actions are no longer lost along the way.
You keep full traceability of every commitment made, with clear dashboards on those responsible, deadlines, status and results.
Quality becomes operational, visible and measurable.
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Your teams supported by an AI-enhanced quality engineer
Learn from every action, improve continuously
Yxir embeds an AI trained on real industrial data to support you in the search for root causes and the detection of recurrences.
It draws on recognized quality methods (5W2H, 5 Whys...) to suggest analysis paths and relevant action plans.
Each anomaly becomes a collective learning opportunity.
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A management and reporting dashboard for each decision-making level
Manage quality performance, site by site
From the field to management, monitor the right indicators at the right level. Visualise the status of resolutions, identify bottlenecks and anticipate drift. With Yxir, you can manage quality at 360°: by site, by line, by type of deviation. Your data becomes a lever for action.
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