Lifesciences
Eliminate Document Chaos, Simplify Compliance, Accelerate Production.
CARA centralises content, document, and process management for manufacturers, so design specs, SOPs, and quality records stay compliant, current, and easy to find.
Unified Content, Document & Process Management for Manufacturing
Centralise critical documentation and make easy to find. Build and automate workflows that reflect the way your business actually runs. So when the inspector calls, everything is already traceable, findable, and provable.
Gain Control of Your Content
Get instant access to the latest documentation; whether it’s engineering drawings, quality reports, or production manuals. Everything is centralised, secure, and easy to find, helping you eliminate silos and avoid costly errors.
Automate Workflows, Accelerate Work
Manual processes slow production down. CARA automates workflows, routes tasks to the right teams, and keeps projects moving. So you can deliver faster, reduce costs, and focus on building quality products.
Stay Compliant, Stay Confident
CARA simplifies compliance by keeping your critical documents like SOPs, product specs, and safety protocols organised, version-controlled, and audit-ready. No more scrambling for approvals or outdated files when it matters most.
Govern Access, Protect What Matters
Role-based permissions ensure only the right people see sensitive drawings, supplier data, or quality records. Every document is tamper-proof, so you can collaborate safely with partners and suppliers without compromising control.
Trusted by regulated organisations globally
Complexity Slows you Down – CARA Clears the Path
Manufacturing runs on precision, but scattered information and manual processes create costly delays. CARA simplifies how you manage critical content and tasks, helping to solve:
Total Control of Critical Content
Keep everything from design files and SOPs, to product specs and compliance documents at your fingertips. CARA’s powerful search, metadata, and version control eliminate document chaos. Find what you need, the moment you need it. No duplicates, no guesswork.
Keep LearningSimplified Compliance & Risk Management
CARA automates document approvals, tracks changes, and logs every action – helping you meet ISO, OSHA, FDA, and other global standards. Be audit-ready, anytime, with confidence built into every workflow.
CARA Compliance
Workflow Automation for Faster Production
Digitise and automate repetitive tasks like change requests, supplier document reviews, and issue reporting. Keep projects moving, reduce delays, and give your teams back valuable time.
Learn MoreEffortless Integration & Scalability
Connect CARA to the ERP, MES, QMS, and CAD/CAM systems you already run — SAP, Oracle, Dynamics, and more — with an open API that extends to virtually any tool in your stack. As you grow across plants, product lines, or acquisitions, CARA’s modular design scales with you, without compromising performance or compliance.
Designed for the real demands of manufacturing
Design Change Requests
Automate approvals and track every update
Supplier & Contract Management
Manage supplier documents and contract terms with full traceability
Quality Incident Reports
Streamline reporting and corrective actions directly from the shop floor
Regulatory Submissions
Ensure Accuracy and completeness, every time.
