Puritan Enviromax and ESK for Surface Sampling



Validation for the New FDA Inspections - Webinar


2018, April 5 @ 10:00 - 11:00

Clinical, Food, Pharmaceutical, Water » Webinar


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

Visit www.compliance4all.com
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407


Venue

Internet - webinar

Organizer

Compliance4All
Phone: +1-800-447-9407
Email: support@compliance4All.com
Visit organizer website



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