Product and input intake
Collect product formulations, input categories, suppliers, facilities, labels, and requested verification scope.
Software for Non-GMO verification programs
Connect Non-GMO inputs, supplier evidence, testing, and approval to every product
Certifable helps Non-GMO verification programs trace products to inputs, suppliers, segregation controls, testing evidence, facility assessments, approval decisions, and current certificates.
The operational cost of the old way
Certification cannot stay trapped in inboxes and spreadsheets
High-risk inputs, supplier declarations, certificates, and test reports are stored separately from the product decision they support.
Segregation and traceability controls are reviewed inconsistently across facilities and supply chains.
Applicants cannot see which input, supplier, or result is preventing approval.
Product changes and evidence expiration create gaps between the certified scope and the current formulation.
A connected Non-GMO workflow
From first submission to current certificate standing
Configure risk-based evidence requirements and keep every approved product connected to the current input, supplier, testing, and facility record.
Risk classification
Apply program-specific evidence requirements to higher-risk crops, inputs, processing aids, and supply-chain paths.
Supplier and testing evidence
Track declarations, certificates, traceability documents, sampling records, results, and expiration dates.
Facility and segregation review
Assess receiving, storage, production, cleaning, traceability, and mass-balance controls through documents and audits.
Decision and corrective action
Resolve failed or unclear evidence, close findings, and give authorized reviewers the complete product case.
Certificate and change control
Maintain approved products, facilities, dates, supplier changes, and renewal evidence under a verifiable certificate record.
Remote and hybrid audit readiness
Review evidence continuously instead of waiting for one annual exchange
Supplier declarations, test reports, traceability records, and facility procedures can be reviewed as they arrive. Program staff can identify evidence gaps before an assessment and complete permitted follow-up remotely. This reduces the time between a changed input and an informed approval decision.
Why certification bodies choose Certifable
Modern operations that reinforce your authority
Risk-based document rules
Require different declarations, certificates, or testing evidence according to the input and program rule.
Product-to-supplier traceability
Connect each product to its current inputs, manufacturers, certificates, declarations, and review status.
Change visibility
See when a formulation, supplier, facility, or evidence record changes before it creates a certificate-scope gap.
Current verification
Let buyers confirm the program's current certificate standing through an issuer-controlled QR record.
Questions from Non-GMO agencies
Fit the platform to your certification program
Certifable supplies the operating system. Your certification body retains control of the standard, interpretation, evidence, audit method, and final decision.
Can evidence rules differ by input risk?
Yes. The program can configure which materials require declarations, certificates, testing, or additional review.
Can test reports and supplier documents be linked to a product?
Yes. Products, inputs, manufacturers, declarations, certificates, and other evidence remain connected within the certification record.
Does Certifable perform laboratory testing?
No. Certifable manages the program's evidence and decision workflow; the certification body defines acceptable laboratories, methods, and thresholds.
Can facilities be audited for segregation controls?
Yes. Configurable audit templates can cover receiving, storage, cleaning, production, traceability, and corrective actions.
How are supplier or formula changes handled?
Changed inputs, suppliers, facilities, and documents can be reviewed against the current approved scope before the certificate is updated.
Plan the business behind the certificate
What does it cost to run a Non-GMO certification agency?
See personnel, expertise, accreditation, travel, software, training, and governance in one transparent planning model.
Related certification software
Your standard. Your portal. Your decision.
Show clients a modern Non-GMO certification experience
Replace fragmented administration with one branded platform that keeps your team, clients, evidence, audits, and certificates connected.