Validation
Validated
AOAC & manufacturer validation
Where a product holds AOAC Performance Tested Method status, we state the exact scope.
Our approach
Built Around Quality & Compliance
Documented
Certificate of analysis per lot
Standards and reference materials ship with lot-specific CoA.
Traceable
Cold-chain & shelf-life handling
Controlled storage and transport for cultures, kits and biological reagents.
Reviewed
Dated technical claims
Claims are reviewed on a rolling basis, with the source named and a review date.
The register
Certifications & Validations
Each entry states the method, the scope and the certificate reference. Underlying documents are supplied on request.
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Validation
AOAC - Kikkoman Easy Plate Coliform Count
Validation
AOAC - Kikkoman Easy Plate EColi Coliform
Validation
AOAC - Kikkoman Easy Plate Staph Aureus
Validation
AOAC - Kikkoman Easy Plate Yeast And Mold Rapid
Validation
AOAC - Nemis N-Light Salmonella Risk Rapid Pathogen Detection
Validation
AOAC - Nemis N-Light L. mono Rapid Pathogen Detection
Validation
AOAC - Kikkoman Hygiene Monitoring LuciPacA3
Validation
AOAC - Kikkoman Easy Plate Aerobic Count Rapid
Validation
AOAC - Kikkoman Easy Plate EnteroBacterieacea
Validation
AOAC - Biolum Hygiene Monitoring System
No certification matches that combination - reset the filters or ask our technical team.
Validation applies to the specific product and named scope - not to a technology in general.
Governance
How We Handle a Technical Claim
01
Source
Obtain the claim from a manufacturer or certification-body document.
Origin
02
Verify
Check the scope - analyte, matrix, limit - matches what we publish.
Scope check
03
Structure
Store it as a record with its reference, not as free text.
Record
04
Display
Show it consistently, with a review date, only where it is supported.
PublishedOur commitment
What we will not do
Three rules that keep every claim on this site honest.
- We do not claim that every product is AOAC validated when only specific products and methods are.
- We do not copy specification values from a manufacturer PDF without verifying them.
- We do not reproduce supplier marketing as evidence.
On request
Documentation We Can Supply
DocumentIssued
AOAC / other validation certificates
Per product
Manufacturer validation and performance reports
Per product
Certificate of analysis
Per lot
Instructions for use and datasheets
Per product
Method-verification support documents
Per product
FAQ
Frequently Asked Questions
What does "AOAC Performance Tested Method" mean?
It means an independent body has evaluated a specific method or kit against defined performance criteria for a named set of analyte–matrix combinations. The certificate states that scope precisely.
Are all Fobeventia products AOAC validated?
No. Specific products hold validation for specific scopes. Where a product is not validated for your exact matrix, we say so and discuss verification options.
Can you provide a certificate of analysis?
Yes - standards and reference materials ship with a lot-specific CoA, and we can supply it ahead of purchase on request.
Do you help with in-house method validation?
Yes. Our technical team supports verification of recovery, precision and detection limits on your own matrices, and the documentation that goes with it. See Our Expertise.
Where do the specification values on product pages come from?
Verified values are structured and stored in our CMS from validated source documents, then displayed consistently - not copied ad hoc from a brochure.
