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| Verification vs. Validation - Product, Process, Software and QMS From GlobalCompliancePanelGlobalCompliancePanel, a leading regulatory and compliance training gateway, will host a two-day, in-person seminar on the topic, “Verification vs. Validation - Product, Process, Software and QMS” on January 17 and 18 at Las Vegas.
The FDA has new and tougher regulatory requirements for a company’s Master Validation Plan for major key inputs and CGMP deficiencies. This seminar will address these. It seeks to demonstrate "Product Risk Based V&V" by sufficient, targeted and documented risk-based V&V test case elements/scripts. It will help participants evaluate these elements against ISO 14971 and ICH Q9 for hazard analysis and product risk management. In arriving at its goal, this seminar will evaluate aspects such as different field-tested, U.S. FDA-reviewed V&V protocols; how to employ equipment/process Requirements Specs/DQs, IQs, OQs, and PQs, or their equivalents per ASTM E2500, all against a background of limited company resources. It will review a matrix that simplifies "as-product" ------------------------------------------------------------ Course Description: Day 1 - 17th January 2013 Lecture 1: Master Validation Planning and the Master Validation Plan(s) Lecture 2: Product, Process/Equipment Hardware V&V Lecture 3: Product/Device V&V Lecture 4: Software V&V Lecture 5: Quality Management System/21 CFR Part 11 V&V Lecture 6: Summary of morning discussion Lecture 7: Group activity on the MVPs Lecture 8: Review of group activity and Q&A Day 2 - 18th January 2013 Lecture 9: Software V&V documentation "model" Lecture 10: Software V&V protocols - "black box", "white box" Lecture 11: Electronic Records and Electronic Signatures (Part 11) Lecture 12: Summary of morning discussion Lecture 13: Group activity on 1) hardware/equipment, and 2) software V&V protocols Lecture 14: Review of group activity and Q&A Lecture 15: Course summary discussion Lecture 16: Summary of morning discussion Lecture 17: Group activity on the MVPs Lecture 18: Review of group activity and Q&A ------------------------------------------------------------ Purpose of the seminar This session helps participants: o Understand Verification and Validation, differences and how they work together; o Discuss recent regulatory expectations; o Know how to document a "risk-based" o Determine key "milestones" o Locate and document key subject "inputs"; o Compile "generic" Master and Individual Validation Plans; o Learn the key element of a Product V&V File/Protocol; o Understand how to develop Process and/or Production/Test Equipment V&V Files/Protocols; o Get a grasp of basic Test Case construction; o Understand sample sizes and their justification; o Learn the key elements of Software V&V expected by the FDA and how to document; o Deal with hardware and software vendors, sales and marketing o Consider a field-tested software V&V documentation "model"; o See how to compile QMS Electronic Records and Electronic Signatures V&Vs to satisfy 21 CFR Part 11. ------------------------------------------------------------ About the Speaker: John E. Lincoln is Principal of J. E. Lincoln and Associates LLC, a consulting company. John, a graduate of UCLA, is a medical device and Regulatory Affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management and U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/ John has also managed pilot production, regulatory affairs, product development/ ------------------------------------------------------------ Who will benefit: This workshop will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning and V&V activities/plan( o Senior and middle management and staff o Regulatory Affairs o Quality Assurance or Quality Control Professionals o QA/QC o IT/IS o R&D o Production Management o Manufacturing Engineers o Process Engineers o Software Engineers o Project Managers o Hardware and software vendors, sales and marketing o Any professional tasked with V&V responsibilities DATE AND VENUE: January 17 and 18, 2013 Seminar Timings: 9am to 6pm EST Venue:Hilton Grand Vacations Suites at the Flamingo Address: 3575 Las Vegas Boulevard South, Las Vegas, Nevada, 89109 Price –$ 1495; Group discounts available in the following pattern: Send two attendees: Get a discount of 10% Send three to six attendees: Get a discount of 20% Send seven to 10 attendees: Get a discount of 25% Send 10 attendees or more off: Get a discount of 30% To avail the above group discounts, all the participants should register by making a single payment.Please contact Customer Care at 1800 447 9407 ------------------------------------------------------------ Contact Information: Event Coordinator Toll free: 1800 447 9407 Fax: 302 288 6884 Email: support@globalcompliancepanel.com Website:https://www.globalcompliancepanel.com/ GlobalCompliancePanel NetZealous USA Livermore Common, Fremont, CA 94539, USA Phone: 1800 425 9407 End
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