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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 | Edit Freely

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 Validate

Process of Verification and Validation

Linkages to your Quality System

Master Validation Planning

Best Practices

Who Will Benefit:

Manufacturing Engineers

Process Engineers

Quality Engineers

Engineering Managers

Auditors

Compliance Specialists

Speaker 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$150.00

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: support@compliance4All.com


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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