ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report Plan PIF Follow-Up Actions: Document follow-up actions

Name: ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report Plan PIF Follow-Up Actions: Document follow-up actions
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Description

Follow-Up Actions: Document follow-up actions from prior MRMs

measuring equipment must be:

Any reference in this Regulation to the competent authority of the Member State in which the manufacturer has its registered place of business shall be understood as a reference to the competent authority of the Member State in which the authorised representative

Supplier Evaluation and Monitoring Procedure

To demonstrate compliance with this section of the standard

ISO 13485 (Clause 8.4) - Post Market Clinical Follow Up (PMCF) Report Plan PIF Follow-Up Actions: Document follow-up actions

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