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Global SOP - DOCUMENTATION MANAGEMENT PROCEDURE

Global SOP - DOCUMENTATION MANAGEMENT PROCEDURE HAEMONETICS CORP. - COMPANY CONFIDENTIAL Before using this document, please consult Agile for the latest revision. Page 1 of 26 Global : Revision: CU Purpose This PROCEDURE provides the minimum requirements for Haemonetics Document Control and Records MANAGEMENT , including issuance, review, authorization and control. Scope This PROCEDURE applies to all world-wide facilities and organizations in Haemonetics, including corporate. This PROCEDURE applies to new documents and document revisions under the MANAGEMENT and control of documents that are part of Corporate DOCUMENTATION as well as Quality MANAGEMENT System (QMS), Design History File (DHF), Device Master Record (DMR) and Device History Records (DHR).

Global SOP - Design Control New Product Design And Release Process SOP15.01 Global SOP-MDD Technical File Requirements SOP15.09 Global SOP-Clinical Investigation Capital , Equipment and Disposables SOP16.09 Global SOP - Temporary Change Notification SOP2529 Agile Training: Navigation, Basic Search And Approve/Reject TI1075

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