QLUTCH QMS · English (International)
Software around your ISO/IEC 17025 laboratory processes — International
Evaluate procedures, learning and records around your laboratory methods. Confirm competence and accreditation requirements with the appropriate body.
Start with your process
- Choose a representative task and identify its owner.
- Walk through the requirements for documents, workflows, training and records.
- Test permissions, exceptions and evidence retrieval.
- Confirm deployment, commercial terms and implementation responsibilities.
Your organisation defines and verifies its requirements. Qlutch does not confer certification, accreditation or regulatory compliance.
Explore the tools
DocControl: controlled documents
Organise controlled procedures around defined versions, review responsibilities and access. Demonstrate your document lifecycle before rollout.
FormFlows: defined workflows
Coordinate the steps, information and responsibilities of a defined process. Test ordinary cases, corrections and exceptions with your team.
Training: learning and assignments
Organise learning and assignments around the responsibilities of your team. Confirm completion evidence and the review process you require.
Lists: structured quality records
Organise structured information in registers that fit your work. Confirm fields, permissions and retrieval using a representative record.
Contact
This edition describes the marketing website. Confirm application and support languages, service availability, data processing and commercial terms with Qlutch for your intended location.
The existing booking, contact form and application destinations may use English. Tell us your preferred language when you contact us.
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