Essentials of Validation -IQ,OQ,PQ - 2017
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 and Presenter Information
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.
Relevant Government Agencies
Validation
Event Type
Webcast
This event has no exhibitor/sponsor opportunities
When
Thu, Sep 14, 2017, 10:00am - 11:30am
PT
Cost
| General Admission: | $150.00 |
Website
Click here to visit event website
Organizer
NetZealous - Compliance4All
