21 CFR Part 820 is a mobile reference tool that provides the full text of the FDA’s Quality Systems Regulation. Developed by Cimcon Software, Inc., it enables practitioners to access regulatory content offline for compliance-related tasks.
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 quality system regulations.
What does it look like?
Key features
Allows users to browse the regulation text 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.
Allows users to send regulatory pages to themselves or colleagues via email.
How much does it cost?
Velocity
Dormant developmentShow more...
4 versions in history. Development pace: zombie.
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 820
How's the Business market?
The rivals identified
The Analyst's Read
Key takeaways for 21 CFR Part 820
Where is it heading?
Bottom line
This app serves as a specialized, portable digital reference for the FDA’s 21 CFR Part 820 regulation.
Report last updated