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Validation for the New FDA Inspections
Thursday, April 5th at 10:00am PST
Online sale ends: 04/05/18 at 9:00am PST
Online
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539
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Talent

Edwin Waldbusser

Description
Overview:
How to conduct a software validation program that will satisfy FDA requirements and produce a safe product.

Why should you Attend:
There are additional requirements,analyses and tests that FDA feels are necessary to prevent user injuries. These requirements were developed after analysis by the FDA of many recalled medical devices. In this webinar you will learn the requirements in addition to functional tests that are required to produce a validated software product. 

Areas Covered in the Session:
Software Validation more than Testing
Requirements Traceability
Risk Analysis
Unit,Integration and System Testing
Algorithm Validation
Challenges to the Software
Configuration Management

Who Will Benefit:
Engineer
Engineer Management
Software Engineer
Programmer
Quality Assurance
Regulatory

Speaker Profile:
Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA.

Event Fee: One Dial-in One Attendee Price: US$150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

http://www.compliance4all.com/control/w_product/~product_id=501817LIVE?channel=purplepass_Apr_2018_SEO
Additional Information
One Dial-in One Attendee Price: $150.00

Presented By

10:00am to 11:00am
Doors open at 8:00am

General Admission: $150.00

Online<br> 161 Mission Falls Lane, Suite 216,<br> Fremont, 94539

18004479407

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