21 CFR Part 211 Guide is a mobile reference tool providing the full text of the FDA’s current Good Manufacturing Practice regulations. Developed by CIMINFO Software, Inc., the app is designed to provide practitioners with portable, offline access to regulatory content.
Overview · Full Intel report in progress
The App DNA
What makes this app unique?
For Professionals working in FDA-regulated industries who require mobile access to 21 CFR Part 211 compliance standards.
What does it look like?
Key features
Allows users to browse the full text of the regulation through an organized structural index.
Enables users to locate specific regulatory content quickly using targeted search terms.
Provides the ability to save specific pages for quick retrieval and future reference.
Supports the distribution of regulatory pages via email to the user or colleagues.
How much does it cost?
Velocity
Dormant developmentShow more...
4 versions in history. Development pace: zombie.
Who built it?
Cimcon Software
13+ apps tracked · Business
NetScale
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Sarbanes-Oxley Act of 2002
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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 211 Guide
How's the Business market?
The rivals identified
The Analyst's Read
Key takeaways for 21 CFR Part 211 Guide
Where is it heading?
Bottom line
This app serves as a specialized, paid mobile utility for professionals needing constant, offline access to FDA 21 CFR Part 211 documentation.
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