Essentials of Validation -IQ,OQ,PQ - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501426LIVE?channel=ourglocal_Sep_2017_SE |
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Category Validation Planning, Quality Webinars, Quality System, software project management, Compliance laboratory information system, Master Validation Planning, Compliance Specialists, Benefits of Process Validation, medical device industry
Deadline: September 13, 2017 | Date: September 14, 2017
Venue/Country: Fremont, U.S.A
Updated: 2017-07-17 16:01:12 (GMT+9)
Call For Papers - CFP
Overview:Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation.You'll learn about what processes needed to be validated and what steps you need to take to validate processes.Why should you Attend:You’ll learn the benefits and impacts of validation and how it can benefit your customers and your business. We’ll cover tools and techniques that can help you successfully validate your processes. Areas Covered in the Session:When to Verify and ValidateProcess of Verification and ValidationLinkages to your Quality SystemMaster Validation PlanningBest PracticesWho Will Benefit:Manufacturing EngineersProcess EngineersQuality EngineersEngineering ManagersAuditorsCompliance SpecialistsSpeaker Profile:Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.Event Cost & Details:One Dial-in One Attendee Price: US$150.00Contact 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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