Quality System
At VARO, quality is not something we inspect at the end of a project. It is an integral part of how we develop, build, and document customized machinery.
ISO 9001 certified
We are ISO 9001 certified, demonstrating that we work systematically with quality assurance, process management, and continuous improvement. For us, certification is more than a formal standard. It reflects a way of working where quality is built into every stage of the process—from the first customer dialogue to the finished solution, documentation, and handover.
We are also ISO 14001 certified and take a structured approach to environmental management and continuous improvement across the organization.
A quality management system built for technically demanding projects
Our quality management system is designed for projects with demanding requirements for documentation, traceability, and process control.
This means that every project follows a documented process with clearly defined phases, responsibilities, and control points. This approach provides transparency and control over technical requirements, regulatory considerations, changes, risks, and approvals throughout the entire project lifecycle.
Our quality management system helps ensure that:
- Design decisions are documented and reviewed throughout the project
- Changes are tracked, assessed, and approved systematically
- Technical requirements and customer requirements are followed throughout the project
- Risks are managed as an integral part of design, testing, and documentation
- Project progress is transparent to both the customer and the VARO project team
Adapted to GMP- and GxP-regulated environments
We have many years of experience delivering solutions to the pharmaceutical, medical device, and other industries where requirements for quality and documentation are extensive.
Our quality management system is structured to support the principles of GAMP 5 and can be adapted to GMP- and GxP-regulated environments when required by the project. This enables us to work with traceability, risk management, testing, and approval workflows in a way that integrates seamlessly with your internal QA and validation processes.
We work closely with your project, QA, and validation teams to ensure that technical requirements, compliance, and operational needs are aligned from the very beginning.
Flexibility within a structured framework
Although we work according to a documented project model, we know that no two customers are alike.
That is why we adapt the level of documentation, formats, review milestones, and approval workflows to fit your organization and compliance structure. Some projects require extensive validation support, while others call for a more streamlined documentation package focused on operation, maintenance, and CE documentation.
What all projects have in common is that quality must be clear, understandable, and fully documented.