Establishing a Reduced Testing Process for Incoming Materials
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Website http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500481?expDate=Ourglocal |
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Category Certificate of Analysis, cGMP regulations, FDA 21 CFR Regulations, GMP Standard, Material Qualification, Medical Device Components, Pharmaceutical Testing, Supplier History, Supplier Qualification, Trending
Deadline: September 24, 2014 | Date: September 24, 2014
Venue/Country: 38868 Salmon Ter, Fremont, U.S.A
Updated: 2014-09-16 19:03:08 (GMT+9)
Call For Papers - CFP
Instructor: Howard T CooperDescription:The first step in reduced testing is to qualify the supplier using the supplier qualification process. This webinar will review the supplier qualification process.The sequential steps for establishing reduced testing program will be presented in a logical way using graphics including flowcharts. Guidance and recommendations for assessing the data to qualify a supplier for reduced testing will be discussed. This will be followed by describing the monitoring process to assure the required reliability. Considerable use of graphics will be used. Additionally, the basic quality principles that apply to reduce testing will be emphasized. Why Should you Attend:To increase understanding of requirementsTo learn how to maintain compliance and increase qualityTo gain insight for improving supplier quality while reducing cost and gaining resources that can be applied to quality, product, and process quality.Objectives of the Presentation:IntroductionThe role of materials in the achievement of product quality and customer satisfactionSimilarities and differences of regulatory requirements for pharmaceutical, medical device, dietary supplements and food.Types of quality certificatesA brief overview of supplier selection and qualificationMaterial and laboratory qualificationMaterial validationCollaborative testing between you and your supplierFactors to consider in establishing the sample plan to reduce riskThe sampling plan calculation based primarily on risk factorsMonitoring analytical resultsTaking corrective actionWorking with the supplierSupplier disqualificationGoing beyond reduced testing to supplier certificationFDA compliance activities related to reduced testingWho can Benefit:QA, QCLaboratoryReceiving warehouseCost AccountingExternal AuditingQuick Contact:http://www.onlinecompliancepanel.com/ecommerce/webinar/~product_id=500481?expDate=OurglocalToll free: +1-510-857-5896Email:?webinaronlinecompliancepanel.comOnlineCompliancePanel LLC,38868 Salmon Ter,Fremont, CA 94536, USA
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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