Personal or health-related
Roles, purposes, access from abroad, subcontractors, retention and deletion.
View health requirements →Guidance by trigger
A questionnaire, an audit, market entry or the maintenance of several engagements each call for distinct decisions and levels of evidence.
Review situationsThe supplier examines its own capability. The European client defines the supplier decision it needs to reach.
Self-assess my organisation →Assess a supplier →Search the platform →Choose an engagement
Start from what needs to be obtained now: an answer, an in-depth review, or a capability tracked over time.
View all engagementsVerify and remediate.
EU exposureClient and technical assessmentEvidence and remediationAll preparations →Keep the current commitments.
Continuous assuranceClient assurance officeProduct security cellAll recurring services →Basis for the conclusions
The same trail links Promise, Policy, Practice, Platform, finding, remediation and controlled sharing.
Review the 4P methodSee fictitious examples to understand the structure and depth of the deliverables.
See examples of deliverables →Terms of engagement
Confidentiality, independence, reversibility and traceability of responsibilities structure the conduct of the work.
Review the firm's rulesHave an international supplier assessed under explicit mandate and sharing rules.
Assess a supplier →Supplier relationships
Qualify what is provided, what the European client entrusts and what genuinely depends on the relationship.
The true scope
A company may manufacture a mechanical part, process health data, develop software or operate an activity for a European client. The analysis starts with the flows and dependencies created by the relationship, not with a sector label.
Service, study, software, device, equipment, component or sub-assembly.
Data, access, plans, code, know-how, procedures or trade secrets.
Continuity, service quality, security, industrial capacity or market access.
Five exposure gateways
Each entry point changes the relevant evidence, the people to interview and the controls to examine.
Roles, purposes, access from abroad, subcontractors, retention and deletion.
View health requirements →Identities, permissions, roles, privileged accounts, logs and access revocation.
View international access →Classification, need-to-know, copies, transfer, return and subcontracting.
See industrial confidentiality →Development cycle, vulnerabilities, documentation and product-specific obligations.
View the Cyber Resilience Act →Concentration, incidents, alternatives, recovery, reversibility and supply chain.
View the supply chain →iKNSA scope
For a prosthesis, an aeronautical part or industrial equipment, iKNSA can examine the protection of data, access, confidential information and supplier commitments. The clinical, mechanical or regulatory compliance of the product falls, where necessary, to separate competent specialists.