CERTIFICATION & COMPLIANCE GUIDE

EAC renewal and surveillance: reassess scope and changes

Read the document, register status and applicable scheme before planning expiry or surveillance work.

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01

Plan from the actual document and scheme

Read the document, register status and applicable scheme before planning expiry or surveillance work. Identify responsible applicant, covered models and factories, required ongoing tasks and changed regulations. Renewal is not a universal automatic extension, and a declaration should not be treated as a certificate with identical duties.

Maintain a change log for design, components, factory, supplier and responsible parties. Present relevant changes and actual production evidence to the responsible participants. Agree whether new tests, assessment or a new document route are needed instead of copying the old validity dates.

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Responsible preparation and decision

Conditional case: production moved after the original assessment. Disclose the new site before renewal or surveillance planning; an unchanged product name does not prove unchanged manufacturing conditions. Do not invent a completed inspection or erase unresolved findings.

Kayra can organize documents and coordinate questions. The responsible applicant, assessment body and laboratory retain their assigned duties. Kayra is not presented as an EAC issuer, regulator or accredited laboratory; preparation does not guarantee acceptance or a date.

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Read the document, register status and applicable scheme before planning expiry or surveillance work.

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Scope and decision verification

Kayra Patent supports requirement analysis, document preparation and process coordination. Conformity or certification decisions belong to the independent body or public authority authorised under the applicable law and programme. Kayra cannot replace that decision or guarantee a certificate. Verify the issuer, scope, dates and any official register entry.

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