2019 - The 6 Most Common Problems in FDA Software Validation and Verification
Date2019-07-22
Deadline2019-07-22
VenueOnline Event, USA - United States
KeywordsPart 11; Annex 11; Software validation
Topics/Call fo Papers
Which data and systems are subject to 21 CFR Part 11 and Annex 11
Why compliance makes good business sense.
Details of FDA regulations/system features as applied to software: security, audit trails, electronic signatures.
Requirements for local, SaaS, and cloud hosting
The 6 Most Common Problems in FDA Software Validation & Verification.
Strategies on how to avoid the most common problems.
Advice on successful validation project staffing.
Avoid 483 and Warning Letters
Why compliance makes good business sense.
Details of FDA regulations/system features as applied to software: security, audit trails, electronic signatures.
Requirements for local, SaaS, and cloud hosting
The 6 Most Common Problems in FDA Software Validation & Verification.
Strategies on how to avoid the most common problems.
Advice on successful validation project staffing.
Avoid 483 and Warning Letters
Other CFPs
- 32nd International Conference on Contemporary issues in Science, Engineering & Management (ICCI-SEM)
- IISTEM- International Conference on Networking, Communication and Computing Technology(ICNCCT)
- IISTEM-International Conference on Electrical, Electronics & Computer Science (ICEECS)
- IISTEM- International Conference on Advances in Business Management and Information Science (ICABMIS)
- IISTEM- International Conference on Advances in Business Management and Information Science (ICABMIS)
Last modified: 2019-05-30 21:35:10