Date :
Place : United States, Fremont
Contact Person:Event Manager
Description:
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: [email protected]Deadline for abstracts/proposals : 5th August 2019
Organized By :Netzealous LLC DBA - Compliance4All
Keynote Speakers :
Venue :Fremont, CA, USA
Check the event website for more details.