Regulatory testing requires data that’s traceable, defensible, and meets internationally recognized standards. For product claims and regulatory submissions, results need to be backed by documented technical competence.
ISO 17025 is the international standard for testing and calibration laboratories. It’s about demonstrating technical competence, maintaining rigorous quality controls, and ensuring every result is traceable and reliable.
Independent, third-party assessors have examined how we work, and we are delighted that the VRS team has renewed ISO 17025 accreditation for a core suite of our antiviral testing services.
What’s Accredited
Our ISO 17025 scope covers the following assays:
- ISO 21702: Antiviral activity on plastics and non-porous surfaces
- ISO 18184: Antiviral activity on textile products
- Suspension Test: Virucidal activity in liquid phase
- Neutralisation Assay: Antibody neutralising capacity
- Antiviral Assay: Compound efficacy screening
- qRT-PCR: Viral quantification and detection
Building on Our Quality Framework
This accreditation complements our existing ISO 9001 certification, creating a comprehensive quality management system. While ISO 9001 ensures consistent service delivery, ISO 17025 specifically validates our technical testing competence.
Together, these standards mean you can trust our processes and have confidence in our data.
What This Means for Your Projects
If you’re developing antiviral products, testing disinfectants, or screening compounds, our ISO 17025-accredited services provide the documented evidence you need for regulatory submissions, product claims, and stakeholder confidence.
The same team, the same expertise, the same commitment to getting your virology research right, with added regulatory assurance.
For more information about our accredited services or to discuss your testing requirements, get in touch.
