LIMS & lab process platform

Manage lab processes digitally. Secure quality, GMP processes, and evidence in an integrated way.

ORELIO connects samples, analyses, approvals, results, interfaces, GMP-relevant workflows, and documentation into a manageable laboratory logic – from day-to-day operations to audit readiness.

Part of VITAVO OS – not an isolated point solution.

ORELIO in VITAVO OS

◇

Intelligence

⚙

Operations

▣

Solution Layer

ORELIO in
VITAVO OS.

This product world provides proven capabilities for lab, quality, and regulated process environments. In the Solution Layer, these capabilities can be combined with other VITAVO building blocks – without diluting ORELIO’s specialist depth.

Quality

Standards, audit paths, GMP processes, and quality logic.

Knowledge

Structure documents, templates, work instructions, and knowledge assets.

Evidence

Ensure evidence, approvals, monitoring data, and auditability.

Classification

A product world with a clear role in VITAVO OS.

ORELIO is the product world for laboratories and regulated quality environments that seek to ensure high process quality, traceable results, secure data, GMP-compliant workflows, and efficient workflows within an integrated LIMS structure.

Product Logic

Within VITAVO OS, ORELIO demonstrates how specialized laboratory and quality requirements are embedded in a transferable organizational logic: data integrity, roles, approvals, interfaces, evidence, monitoring processes, and documented responsibilities.

Value Contribution

Business requirements are transformed into reusable templates for roles, workflows, approvals, evidence, reporting, integration, and regulated process management.

Scalability

The solution can integrate with existing systems and be deployed wherever organizations need greater control, traceability, and quality assurance in laboratory and process environments.

Capabilities

What ORELIO makes operationally possible.

The product page explains not only the features, but also the underlying principles: structure, accountability, traceability, quality assurance, and management perspective.

Samples & Analyses

Samples, tests, analyses, and results are clearly assigned and tracked in a traceable manner.

Approvals & Data Integrity

Authorizations, confirmations, result approvals, and documentation are kept under control.

GMP Process Management

GMP-relevant processes, responsibilities, approvals, documentation, and evidence are managed in a structured manner—ensuring that quality is built into the workflow rather than only becoming apparent during an audit.

Environmental Monitoring

Monitoring plans, measurement points, sampling, limit values, deviations, and corrective actions are coordinated in a traceable manner – from data collection to evaluation.

Interfaces & Devices

Existing systems, locations, and hardware can be integrated into the laboratory workflow.

Transparency & Analysis

Result data, status information, monitoring data, and analyses are made available to teams, quality assurance, and management.

Application logic

Specific areas of application.

The following areas highlight where the product world is technically relevant—without duplicating the overarching solution and industry pages.

Laboratory and Analytical Processes

Sample receipt, analysis, result tracking, testing, and approval.

GMP Processes

GMP-relevant procedures, roles, approvals, documentation, and evidence are managed in a controlled and traceable manner.

Environmental Monitoring

Monitoring plans, measurement points, sampling, limit values, deviations, and corrective actions are coordinated in a structured manner.

Quality & Compliance

Audit-proof documentation, access permissions, data integrity, and traceability.

Scalable Testing

Structured handling of large volumes of samples, tests, analyses, and results processing.

Knowledge & Training

Minimal training required, clear user interfaces, documented workflow logic, and traceable work instructions.

VITAVO OS

Product experience becomes organizational logic.

ORELIO remains clearly recognizable as a product world. At the same time, it becomes clear which capabilities are transferable: roles, statuses, approvals, documentation, evidence, reporting, integration, monitoring logic, and regulated process management.

Roles

Workflows

Evidence

Reporting

Integration

  • Laboratory Information Management System for Lab 4.0

  • Structured sample, analysis, and results processes

  • GMP-compliant process management with roles, approvals, documentation, and evidence

  • Environmental Monitoring with Monitoring Points, Threshold Values, Deviations, and Actions

  • Cloud-based data storage and location-independent processing

  • Interfaces to existing systems, devices, and hardware

  • High transparency and traceability in laboratory, quality, and monitoring processes

Product worlds

Organizational & workflow control

Quality, knowledge & evidence

Safety, risk & regulated operations

The next step

Let’s talk about the right application.

During an introductory meeting, we’ll determine how ORELIO can be integrated into your processes, systems, and VITAVO OS architecture.

Zwei Damen sitzen mit Laptops im Besprechungsraum und lächeln sich zu.