ComplianceOnline, Renaissance Orlando Airport Hotel, FL
2016-08-18
If you are looking for the answer to the following questions, you will certainly benefit from attending this seminar on building a vendor qualification program: Have you wasted hours, days, and weeks on qualifying vendors that you know cannot or will not meet your requirements? Has your approach to vendor qualification and vendor audits left you with internal CAPAs, customer audit items, or 483 observations? Have you wondered whether an onsite vendor audit is necessary in the eyes of FDA?
Learning Objectives: This course on vendor qualification program for FDA regulated industries will:
Define a sustainable structure for a vendor qualification program. Explain how change control and other quality programs feed into the vendor qualification program. Offer usable audit forms/checklists and other vendor qualification program document templates.
Who Will Benefit: This course will provide valuable assistance and guidance to all FDA regulated companies for building sustainable vendor qualification program. The following job titles/ positions will benefit from attending this seminar:
Internal Auditors Regulators Legal Departments Compliance Officers Purchasing Managers QC Managers
Note: Use coupon code NB5SQH8N and get 10% off on registration.
For Registration: http://www.complianceonline.com/vendor-qualification-program-for-fda-regulated-industries-requirements-seminar-training-80162SEM-prdsm?channel=hum-molgen
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Invited Speakers:
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Jonathan M. Lewis
Founding Partner, Reliant FDA Experts™…a Division of Advanced Biomedical Consulting, LLCJonathan M. Lewis, founding partner, Reliant FDA Experts™ - a division of Advanced Biomedical Consulting, LLC, has over nineteen years’ experience in the areas of quality control/quality assurance (QA/QC), regulatory affairs, manufacturing, validation, project management, and executive management in both the industry and in consulting roles. Mr. Lewis has experience in the medical device, diagnostic, biopharmaceutical, pharmaceutical, cosmetic, nutritional supplement, food, and animal food industries. Prior to founding Reliant FDA Experts™, Mr. Lewis worked for KMI/PAREXEL, a regulatory compliance and validation consulting firm, in increasing roles of responsibility from an entry-level validation engineer to the associate director of consulting. He has worked at RPScherer (Cardinal Health), a contract and proprietary solid oral dose pharmaceutical manufacturing facility, as the QC/validation manager. In addition, he has worked at Telectronics Pacing Systems, a medical device manufacturer, as a sterility assurance laboratory technician.
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