Review the fit
We review your standards, current workflow, accreditation requirements and the cases you need to manage.
Manage applications, audit planning, documents, approvals and surveillance in one connected system, built inside a working certification body.
Tell us what you want to improve. We'll show the relevant workflow and discuss what adoption would involve.
14
enforced phases
15+
generated forms
8
ISO standards
Certification record
ISO 9001:2015 · UAF
Certification progress
9 of 9 completeApplication received
9 Sep 2025
Planning
10 Sep 2025
Quotation signed
12 Sep 2025
Agreement confirmed
15 Sep 2025
Document review
15 Sep 2025
Stage 1 audit
14 Oct 2025
Stage 2 audit
25 Nov 2025
Committee review
2 Dec 2025
Certificate issued
15 Dec 2025
Certificate expires
14 Dec 2028
Lead auditor
Anna Kowalski
Stage 1 & Stage 2
Certiva was developed in the team's own certification-body operating environment. That is first-hand product experience, not an independent customer endorsement. The organization is unnamed here.
A concrete workflow change
Manual handoff: Application details have to be carried into document templates. In Certiva: an application creates a case, and known details can populate prepared audit documents for staff review.
This is a product workflow example, not a measured result from the operating organization. We do not publish a time-saving figure or named customer case without supporting records and permission.
The configuration and migration plan is agreed around your procedures and records before a launch date is set.
We review your standards, current workflow, accreditation requirements and the cases you need to manage.
Together we agree which templates and settings need configuration, which records can be imported and what remains manual.
Relevant staff learn their roles and work through an agreed case before launch. Your team confirms that the configured flow matches its procedures.
We agree the launch sequence, responsibilities and support arrangements in the implementation proposal.
Your team supplies and approves its source records, templates and procedures. Import feasibility, manual cleanup, configuration limits, support terms and charges are specified in the proposal; they vary by implementation.
Certiva can prepare documents in a certification body's own templates. We review each template and agree the mapping and any adaptation before implementation.
That depends on the format, quality and structure of your current records. We assess a sample, define the fields and files in scope, and identify anything that needs manual preparation or entry.
Access is organized by role, including separate workspaces for certification staff, auditors and clients. We review the proposed roles, hosting and data-handling terms with you before launch.
Documents can be downloaded from the workflows that produce them. We confirm the record types, formats and any bulk export requirements in the implementation scope.
Onboarding is scoped around configuration, template mapping, agreed data preparation, training, workflow validation and launch support. The exact deliverables are set out in your proposal.
We quote the subscription period and scope, implementation work and any optional custom work separately after reviewing your requirements. The proposal states charges and exclusions before you commit.
Purpose-built for certification bodies operating under ISO/IEC 17021-1.
Explore product views rebuilt from Certiva's working demo environment using synthetic company data.
One live record
Follow a certification from application to certificate with the full evidence trail attached to the same record.
Certification record
ISO 9001:2015 · UAF
Certification progress
9 of 9 completeApplication received
9 Sep 2025
Planning
10 Sep 2025
Quotation signed
12 Sep 2025
Agreement confirmed
15 Sep 2025
Document review
15 Sep 2025
Stage 1 audit
14 Oct 2025
Stage 2 audit
25 Nov 2025
Committee review
2 Dec 2025
Certificate issued
15 Dec 2025
Certificate expires
14 Dec 2028
Lead auditor
Anna Kowalski
Stage 1 & Stage 2
Controlled workflow
Applications, planning, audits, reviews, decisions, certificates and surveillance stay connected through defined workflow gates.
Complete record
Known case data can populate forms. Signatures, findings, evidence and approvals remain linked to the relevant record.
Audit-ready evidence
The system records workflow changes and related approvals, helping your team examine the basis for each decision.
CertivAI prepares the work and shows its reasoning. Your team reviews, changes, and approves every result.
AI report
JOB-CASCADE-2025-002
Report ready
Standards
ISO 9001
Report context
Stage 2
Accreditation body
UAF
Company
Cascade Metal Fabrication
Evidence package
23 documents
Duration
8m 42s
Report ready
Generated in your DOCX template and ready for auditor review.
Multi-standard by design
Bring your standards and document set. We'll show you how the complete workflow fits your certification body.