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ISO 13485 (Clause 8.2) - Internal Audit Schedule (By Documentation) Template

ISO 13485 (Clause 8.2) - Internal Audit Schedule (By Documentation) Template

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ISO 13485 (Clause 8.2) - UK Vigilance and Reporting to the Regulatory Authorities Procedure

ISO 13485 (Clause 8.2) - UK Vigilance and Reporting to the Regulatory Authorities Procedure

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ISO 13485 (Clause 8.2) - USA Medical Device Vigilance and Reporting for Manufacturers

ISO 13485 (Clause 8.2) - USA Medical Device Vigilance and Reporting for Manufacturers

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ISO 13485 (Clause 8.2) -Singapore Vigilance and Reporting to the Regulatory Authorities

ISO 13485 (Clause 8.2) -Singapore Vigilance and Reporting to the Regulatory Authorities

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ISO 13485 (Clause 8.3) - Issue Report Form

ISO 13485 (Clause 8.3) - Issue Report Form

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ISO 13485 (Clause 8.3) - Medical Device Rework Report Template

ISO 13485 (Clause 8.3) - Medical Device Rework Report Template

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ISO 13485 (Clause 8.3) - Non-Conformance Log Template

ISO 13485 (Clause 8.3) - Non-Conformance Log Template

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ISO 13485 (Clause 8.3) - Non-conformance Procedure Template

ISO 13485 (Clause 8.3) - Non-conformance Procedure Template

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ISO 13485 (Clause 8.3) - Non-conformance Report Template

ISO 13485 (Clause 8.3) - Non-conformance Report Template

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ISO 13485 (Clause 8.3) - Rework Procedure Template

ISO 13485 (Clause 8.3) - Rework Procedure Template

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ISO 13485 (Clause 8.3) - Rework Protocol Template

ISO 13485 (Clause 8.3) - Rework Protocol Template

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ISO 13485 (Clause 8.4) - Annual Measurement and Analysis Report

ISO 13485 (Clause 8.4) - Annual Measurement and Analysis Report

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ISO 13485 (Clause 8.4) - Measurement and Analysis Report Plan

ISO 13485 (Clause 8.4) - Measurement and Analysis Report Plan

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ISO 13485 (Clause 8.4) - Monitoring, Measurement & Post Market Activities Procedure (Class I)

ISO 13485 (Clause 8.4) - Monitoring, Measurement & Post Market Activities Procedure (Class I)

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ISO 13485 (Clause 8.4) - Monitoring, Measurement & Post Market Activities Procedure (Class II+)

ISO 13485 (Clause 8.4) - Monitoring, Measurement & Post Market Activities Procedure (Class II+)

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ISO 13485 (Clause 8.4) - Periodic Safety Update Plan

ISO 13485 (Clause 8.4) - Periodic Safety Update Plan

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ISO 13485 (Clause 8.4) - Periodic Safety Update Report

ISO 13485 (Clause 8.4) - Periodic Safety Update Report

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ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report

ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report

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ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report Plan

ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report Plan

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ISO 13485 (Clause 8.4) - Post Market Surveillance Report

ISO 13485 (Clause 8.4) - Post Market Surveillance Report

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ISO 13485 (Clause 8.4) - QMS Objectives Annual Report

ISO 13485 (Clause 8.4) - QMS Objectives Annual Report

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ISO 13485 (Clause 8.5) - CAPA - Corrective & Presentative Action Report Log

ISO 13485 (Clause 8.5) - CAPA - Corrective & Presentative Action Report Log

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ISO 13485 (Clause 8.5) - CAPA - Corrective and Preventative Action Report Form

ISO 13485 (Clause 8.5) - CAPA - Corrective and Preventative Action Report Form

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ISO 13485 (Clause 8.5) - CAPA Procedure

ISO 13485 (Clause 8.5) - CAPA Procedure

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