Software Validation for Medical Instrument Development [Introduction]

Date Aug 7, 2019
Time 10:00 AM to 11:00 AM
Cost 150.00
Online
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@gmail.com

 


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