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Global SOP - DOCUMENTATION MANAGEMENT PROCEDURE
Responsible for w atermark ing p revious revision of items on the workflow as “Superseded”. This does not apply to Parts, MI and SI. Responsible for approving/releasing labels in the Robar system. Manages notification of periodic document reviews. Document Owner
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The European Medical Devices Regulation 2017/745 The ...
haemonetics.csod.comresponsibilities are delegated to the BUs Implementation of MDR/IVDR is a large and complex project that affects all areas of the business and requires a strong PMO to maintain oversight and strong senior management support to move it forward Supply Chain Lack of transparency in the supply chain challenges the identification and