How software requirements are used in validation

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Category Software Validation, Quality assurance, Risk analysis, Regulatory Affairs Courses Online, development of medical devices, latest software updations

Deadline: January 29, 2018 | Date: January 30, 2018

Venue/Country: Online, U.S.A

Updated: 2017-11-29 15:29:13 (GMT+9)

Call For Papers - CFP

This course is NOT a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.

Why should you Attend:

Testing software to prove that it works and has no bugs is not sufficient to obtain FDA approval. There are additional requirements,analyses and tests that FDA feels are necessary to prevent user injuries.

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.

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

Contact Detail:

Compliance4All DBA NetZealous,

Phone: +1-800-447-9407

Email: supportcompliance4All.com