AquaVerify
AquaVerify standard kits support laboratories working with ISO 10705-2 and EPA coliphage testing workflows.
Standard ISO and EPA coliphage testing kits Technical datasheet
AquaVerify ISO/EPA kits group technical workflows for laboratories working with standardized methods, documentary references or water microbiology control requirements. They can help organize preparation, reading, traceability and digital evidence with AquaVerify Cloud. They do not by themselves determine regulatory acceptance or suitability for a specific regulated use: use depends on matrix, method, documentation, country, competent authority and laboratory scope.
| Field | ISO/EPA kits proposal |
|---|---|
| Workflow type | Technical, documented and aligned with reference methods |
| Recommended user | Advanced laboratories, utilities and regulated-control teams |
| Key documentation | Method, matrix, batch, controls, result and CoA |
| Cloud connection | Audit trail, CoA, review and documentary traceability |
| Related references | ISO 10705-2, EPA 1601/1602 only if applicable to the specific product |
| Prudent note | Do not claim regulatory acceptance by default |
The standard kit range is built for teams that need method alignment, repeatability and technical confidence.
AquaVerify helps laboratories connect technical methods with digital sample and report traceability.
No. ISO/EPA references should be understood as technical alignment or workflow support when product documentation justifies it. Regulatory acceptance depends on the competent authority, exact method, matrix, controls, laboratory and scope.
AquaVerify Cloud can help document sample, batch, operator, method, result, evidence, review and CoA. This supports traceability and documentary auditability, but it does not replace quality-system requirements or technical method review.
References to ISO 10705-2, EPA 1601 or EPA 1602 should be used only when the product and applicable technical documentation support them. Public content should speak about workflows aligned with or related to reference methods, not automatic equivalence.
The laboratory should review target organism, matrix, procedure, controls, technical documentation, accreditation requirements, competent authority and intended use. It should also define how evidence, batches and reviews are recorded.
They can support control programs when they fit the sampling plan, method and technical scope. The decision should be documented and reviewed within the framework applicable to the country, sector and laboratory.
