21 CFR Part 11 is a mobile reference tool that provides the full text of the FDA’s regulation regarding electronic records and signatures. Developed by Cimcon Software, Inc., it serves as a portable resource for industry practitioners to access regulatory content on the go.
Overview · Full Intel report in progress
The App DNA
What makes this app unique?
For Professionals working within FDA-regulated industries who require mobile access to 21 CFR Part 11 compliance standards.
What does it look like?
Key features
Allows users to browse the regulation text through an organized table of contents.
Enables users to locate specific regulatory content using keyword queries.
Provides the ability to save specific pages of interest for quick future reference.
Supports sending regulatory pages via email to the user or colleagues.
How much does it cost?
Velocity
Dormant developmentShow more...
5 versions in history. Development pace: zombie.
Who built it?
Cimcon Software
13+ apps tracked · Business
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NetScale
Basel Framework 2021
Data Integrity Guidance
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Sarbanes-Oxley Act of 2002
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21 CFR Part 58
21 CFR Part 210
Solvency 2 Directive 2009
Basel III Reference Guide
Model Risk Management SR 11-7User Sentiment
What do users think recently?
How are ratings & reviews evolving?
Not enough recent reviews to extract reliable themes yet.
Read the full review analysisCompetition
Competitive landscape for 21 CFR Part 11
How's the Business market?
The rivals identified
The Analyst's Read
Key takeaways for 21 CFR Part 11
Where is it heading?
Bottom line
This app functions as a static, mobile-accessible digital handbook for the FDA's 21 CFR Part 11 regulation.
Report last updated