2019 - Software Validation for Medical Instrument Development [Introduction]

Overview:
This is an introduction to software validation for medical device development targeted to software developers, engineers, testers and managers.
Why should you Attend:
We will discuss the main elements software validation for Medical Instrument Development to deliver testing results complying with these regulations.
Areas Covered in the Session:
Lifecycle and FDA guidance
Stress Testing approaches
Defect tracking and managing
Regulatory and Compliance needs for each phase
Who Will Benefit:
Software Managers
Software Engineers
Test Engineers
Quality Engineers
Quality Scientists
Speaker Profile:
Robert (Bob) Uleski has developed and led projects over the past 40 years for 11 clinical chemistry systems, 5 immunoassay systems, 2 hematology automated analyzers, and 3 laboratory data management systems.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14-AT-gmail.com