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Key deadlines

Conference starts:

2017-09-14

Website

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Conference Description

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