Effective Supplier Qualification Program - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501324LIVE?channel=ourglocal_Aug_2017_SE |
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Category Manufacturing, Vendor Management Checklist, Compliance procurement process, procurement system checklist, procurement software programs, online compliance programs, supplier maangement courses
Deadline: August 02, 2017 | Date: August 03, 2017
Venue/Country: Online, U.S.A
Updated: 2017-06-15 15:10:14 (GMT+9)
Call For Papers - CFP
Overview:FDA considers the supplier as an extension of your operation. You are liable for supplier’s conduct. FDA will deal with your company in case of product failure, especially as related to end user or patient safety concerns. Areas Covered in the Session:Learn the pre-selection, selection and assessment process through the use of various toolsMethods, techniques and strategies that work and are proven with supplier relations and qualificationLearn how to apply risk-based approaches and why and how to "rank" suppliersSupplier Agreements, Quality Agreements and other documentation including Audits/Assessments Who Will Benefit:QA/QC/Compliance/Regulatory AffairsEngineering/R&D/Technical ServicesPurchasing/Procurement/SourcingConsultants Speaker Profile:David R. Dills,Global Regulatory Affairs & Compliance Consultant currently provides regulatory affairs and compliance consultative services for early-stage and established Class I/II/III device, IVD, biopharmaceutical, cosmetics and nutraceutical manufacturers on the global landscape, and has an accomplished record with more than 27 years of experience in the areas of Regulatory Affairs, Compliance and Quality Systems.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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