Material Review Board - 1261 Words

Material Review Board (MRB) ------------------------------------------------- Top of Form Quick Link Bottom of Form Scope This procedure covers determining the disposition of MRB material and identifying corrective action to prevent future discrepancies. Policy The Material Review Board (MRB) consists of representatives from the following departments: * Manufacturing Engineering * Materials * Quality * Purchasing Only the Material Review Board (MRB) can disposition material that fails inspection - that is, only MRB can decide to * scrap material * rework completed assemblies * transfer MRB material to stock * return purchased items to the supplier (including customer-supplied production†¦show more content†¦Refer to Moving Material from Receiving Inspection to MRB [../FND/@PRO1191Y]. For production material rejected from quality inspection, an Inspection Tag and a copy of the DMR are attached to the material. For customer returns rejected from quality inspection, an Inspection Tag, a copy of the DMR, and a copy of the Returned Material Authorization are attached to the material. The original DMR is filed in the MRB suspense file. The job title Material Review Board refers to the following: * Inventory Control Manager * Manufacturing Engineering Manager * Production Control Manager * Purchasing Manager * Quality Manager The job title Inspector refers to one of the following: * Receiving Inspector * Quality Inspector Quality Manager 1. Determine whether any MRB material requires disposition. Oracle Inventory N gt; On-hand, Availability gt; On-hand Quantity Find On-hand Quantities * Check on hand quantities for the MRB subinventory. Oracle Work in Process N gt; Report Submit Requests * Select the WIP Location Report * Check for assemblies in the reject intraoperation step. If any MRB material requires disposition, goto task #3. Otherwise, goto task #2. 2. Cancel the MRB meeting. * Contact the MRB members to inform them that there is no MRB material to disposition today. End of activity. 3. Pull the MRB documentation. *Show MoreRelatedThe Common Rule and Human Research Essay1512 Words   |  7 Pagesmaltreatment of human subjects from the Syphilis Study at Tuskegee (Iltis, 2011). Some key requirements of the Common Rule are: assuring compliance by research institutions, obtaining and documenting informed consent, Institutional Review Board (IRB) membership, function, operations, review or research, and record keeping. 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