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Some large companies, like Proctor & Gamble, develop their own metrics for what they consider to be Good Manufacturing Practices (GMPs) and will conduct audits with their suppliers to ensure that they adhere to them. I worked with a company that was/is a supplier to P&G and they were required to conduct an annual audit (including the support software) and were required to score above 92% compliance or they could lose part or all of their contracts with P&G. The criteria used for the BPCS audit was that any process that affected or touched the product during manufacture had to have a written procedure (usually supported with screen scrapes) and must be audited by the "owner" of that process, with a sign-off sheet validating each step. The scope started with MRP planning (to validate purchase and shop order quantities and timing) and included Purchasing, Shop Floor Control, QMS (if being used), Receiving and Shipping. Sometimes Month End Processing procedures were included, but not always. You should contact your plant manager and find out exactly what the requirements are, because different companies may be using different levels of validation. I hope this helps. Frederick C. Davy, CPIM, PMP Business Systems Analyst Interface Solution, Inc. Phone: (315) 592-8101 Fax: (315) 592-8481 e-mail: fcdavy@xxxxxxxxxxxx Al Mac <macwheel99@xxxxxxxxxxx> Sent by: bpcs-l-bounces+fcdavy=sealinfo.com@xxxxxxxxxxxx 04/13/2006 06:57 AM Please respond to "SSA's BPCS ERP System" <bpcs-l@xxxxxxxxxxxx> To "SSA's BPCS ERP System" <bpcs-l@xxxxxxxxxxxx> cc Subject Re: [BPCS-L] Validating or system calibration What to the letters GMP stand for? It may be helpful for you to consider sub-topic: In a later e-mail, if this is deemed on-topic for BPCS, I may share ANOTHER related sub-topic for consider. * Dirty Data ... for any ERP to work well, you have to have certain very high percentages of accuracy with inventory, factory work reporting, engineering etc. To the extent that you tolerate errors in BOM, scrap reporting, inventory inaccuracies, lead time violations, etc. this is like sabotage for your ERP system. It can be important for a company to have a sense of how accurate your data is, then based on your findings prioritize what to fix. So for example, we have conducted what we call ITEM AUDITS. A small number of items of different types, classes, complexities, are selected. The engineering is carefully examined. Is this 100% correct? If not, it is fixed, and the audit shows that it had to be fixed, and also what the implications were ... had this sabotaged our inventory accuracy? (BOM not right). Had it sabotaged our costs (routings not right)? We do cycle count ... is the on_hand bang on correct, or did we have to adjust the inventory? For different kinds of things, different kinds of processes are needed to measure the accuracy. Now combine the results of this audit with ERP education on what levels of accuracy was needed for the ERP to work right in the first place, and you end up with a Grade ... I not remember what the scores represented exactly, but the goal is to be an A-Class enterprise, and most companies fall far short of this. : >Dear BPCS professional > > > >Recently, I am being asked by our plant manager regarding to their GMP >audit. One of the finding is BPCS calibration or validation to ensure >that system is still running well. Does SSA have this kind of service? >Is it true that GMP should be like that ? > > > >Thanks > > > >Kusman LIM
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