BEGIN:VCALENDAR PRODID:NingEventWidget-v1 VERSION:2.0 METHOD:PUBLISH BEGIN:VTIMEZONE TZID:America/New_York X-LIC-LOCATION:America/New_York BEGIN:DAYLIGHT TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:EDT DTSTART:19700308T020000 RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU END:DAYLIGHT BEGIN:STANDARD TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:EST DTSTART:19701101T020000 RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU END:STANDARD END:VTIMEZONE BEGIN:VEVENT UID:2140535:Event:471134 DTSTAMP:20260411T012305Z SUMMARY:Supplier Quality Remediation using Principles of Lean Document s and Lean Configuration DESCRIPTION:Based on lean manufacturing and documentation concepts, th is webinar deconstructs the supplier quality remediation process.\nWhy Should You Attend:\nDoes your Supplier Quality remediation process re semble the very mess that it is trying to resolve? Receiving Inspectio n (RI) and First Article Inspection (FAI) may appear to be the beginni ng of the manufacturing process. In fact, they are the end deliverable s of the Supplier Quality Management Process which feed into the manuf acturing line. More precisely, they are the objective evidence that th e correct parts were delivered.\nRemediation is a retrospective recons truction of that process. While one may be tempted to focus on the tec hnical details of part and process specifications, one must not lose s ight of the fact that remediation itself is a process.\nTypical remedi ation practices are not managed as a process as one would understand t he term. It has many fluid and moving decisions and ever-changing rule s which are as good as the last meeting or the last conversation, not all of which are documented, not all of which every team member is pri vy to, and not all of which are communicated properly. Does this sound familiar? This webinar can help you!\nA process has distinct inputs a nd outputs, distinct workstations, PARTS*** moving through it, distinc t roles and responsibilities defined at each step, it has \"traffic si gnals\" and controls in place to make sure certain things have happene d before those parts move on to the next step. It also involves resour ce allocation and movement to address bottlenecks. It means having the correct information and asking the right questions at the right time. Not tribal knowledge, nor dependent upon the memory of one person, no matter how experienced, intelligent, or talented that person may be. A swim lane diagram does not have parts, controls, and signals, or act ive bottleneck resource management. It does not have workstations, and it is not the living and moving thing that a process is.\nA swim lane diagram is NOT a process. It is a map and depiction of the process fl ow, but it is NOT the process itself. Also, a tracker is not a process . It is at best a score board but not a substitute for the real thing. \nThis webinar deconstructs the supplier quality remediation process b ased upon lean manufacturing and documentation principles.\n\nAreas Co vered in the Webinar:\n\nPart 1 – Success begins with proper discove ry\nExamining documents, work instructions, specifications, process co ntrols, BOMs, routers, etc.\nElements of lean documents and lean confi guration and their role\n\n\n\n\nWho Will Benefit:\nManagers, Supervis ors, Directors, and Vice-Presidents in the areas of:\n\nQuality Assura nce Departments\nRegulatory Affairs Departments\nManufacturing Departm ents\nEngineering Departments\nResearch and Development Departments\nC ompliance Departments\nProduction Departments\nDocumentation Departmen ts\nOperations Departments\nMedical Device Software Engineers\nMedical Device Software Validation Departments\nMedical Device Software Compl iance Engineers\nDocument Control Teams\nDesign Engineers\nDesign Assu rance\n\n\n\n\nFor more information visit https://medtechiq.ning.com/e vents/supplier-quality-remediation-using-principles-of-lean-documents DTSTART;TZID=America/New_York:20220114T100000 DTEND;TZID=America/New_York:20220114T130000 CATEGORIES:webinar LOCATION:online WEBSITE:https://www.complianceonline.com/supplier-quality-remediation- lean-documents-configuration-webinar-training-706777-prdw?channel=MedT ech%20I.Q URL:https://www.complianceonline.com/supplier-quality-remediation-lean -documents-configuration-webinar-training-706777-prdw?channel=MedTech% 20I.Q CONTACT:8887172436 ORGANIZER:Complianceonline ATTACH;FMTTYPE="image/jpeg":https://storage.ning.com/topology/rest/1.0 /file/get/9982848070?profile=original ATTENDEE;ROLE=REQ-PARTICIPANT;PARTSTAT=ACCEPTED;RSVP=TRUE;CN=Complianc eOnline:https://medtechiq.ning.com/profile/Referral512 END:VEVENT END:VCALENDAR