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2018 - Drafting a Software Verification and Validation Report Package and Protocol - The 11 Must-have Documents
Date2018-06-19
Deadline2018-06-19
VenueOnline event, USA - United States 
KeywordsSoftware V&V documentation pac; Software V&V template
Topics/Call fo Papers
Major industry failures
Tougher FDA expectations / requirements
Roles of verification and validation
The 11-element FDA model - and where it's required
A typical software V&V protocol / test report
A brief overview of 21 CFR Part 11, ER / ES
Legacy, hybrid, new, and cloud systems
Expected regulatory deliverables
Complementary guidelines, e.g., GAMP
Tougher FDA expectations / requirements
Roles of verification and validation
The 11-element FDA model - and where it's required
A typical software V&V protocol / test report
A brief overview of 21 CFR Part 11, ER / ES
Legacy, hybrid, new, and cloud systems
Expected regulatory deliverables
Complementary guidelines, e.g., GAMP
Other CFPs
- International Conference On Statistics & Mathematics
- International Conference on Future Trends in Production, Engineering, Information Technology, Applied Sciences & Bioinformatics
- International Conference on Modern Trends in Biotechnology, System Modeling, Applied Sciences, Engineering & Technology
- International Conference on Recent Trends in Engineering Management, Information Technology, Networking & Applied Sciences
- International Conference on Recent Innovations in Biotechnology, System Engineering, Applied Sciences, Space Environment & Aviation Technology
Last modified: 2018-05-29 02:40:40