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HUM-MOLGEN
-> Events
-> Courses and Workshops |
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April 18, 2017 |
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Compliance4All, Online
2017-06-08
Overview:
This course will teach how to conduct a software validation program that will
satisfy FDA requirements and produce a safe product.
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
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
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Organized by:
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Compliance4All |
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Invited Speakers:
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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.
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Deadline for Abstracts:
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2017-06-07
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Registration:
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Full Details & Registration Link: http://www.compliance4all.com/control/w_product/~product_id=501307LIVE?channel=hum-molgen_Jun_2017_SEO
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E-mail:
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support@compliance4All.com
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