21 CFR Part 58 is a mobile reference tool designed to provide practitioners with offline access to the FDA’s Good Laboratory Practice for Nonclinical Laboratory Studies regulation. Developed by CIMCON Software, the app includes navigation and utility tools to assist professionals in accessing regulatory text on the go.
Overview · Full Intel report in progress
The App DNA
What makes this app unique?
For Professionals and practitioners working within FDA-regulated industries who require mobile access to 21 CFR Part 58 documentation.
What does it look like?
Key features
Allows users to navigate the full text of the regulation through a structured index.
Enables users to locate specific content within the regulation using search terms.
Provides the ability to save specific pages of interest for quick future reference.
Allows users to send regulatory pages to themselves or colleagues via email.
How much does it cost?
Velocity
Dormant developmentShow more...
3 versions in history. Development pace: zombie.
Who built it?
Cimcon Software
13+ apps tracked · Business
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NetScale
Basel Framework 2021
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Sarbanes-Oxley Act of 2002
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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 58
How's the Business market?
The rivals identified
The Analyst's Read
Key takeaways for 21 CFR Part 58
Where is it heading?
Bottom line
While the app aims to provide a convenient mobile reference for FDA regulations, recent user feedback indicates significant technical issues with content accessibility.
Report last updated