21 CFR Part 210 is a mobile reference tool designed to provide practitioners with offline access to the full text of the FDA’s current Good Manufacturing Practice regulations. Developed by Cimcon Software, Inc., the app facilitates regulatory compliance through navigation and content-sharing tools. It serves as a portable resource for professionals operating within FDA-regulated industries.
Overview · Full Intel report in progress
The App DNA
What makes this app unique?
For Professionals and practitioners working in FDA-regulated manufacturing environments.
What does it look like?
Key features
Allows users to browse the full text of the regulation through a structured table of contents.
Enables users to locate specific regulatory content using keyword queries.
Provides the ability to save specific pages for quick future reference.
Supports sending regulatory pages via email to the user or colleagues.
How much does it cost?
Velocity
Who built it?
Cimcon Software
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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 210
How's the Business market?
The rivals identified
The Analyst's Read
Key takeaways for 21 CFR Part 210
Where is it heading?
Bottom line
This is a paid mobile reference tool for FDA regulations that currently faces user feedback regarding the currency of its content.
Report last updated