Skip to main content
Live Webinar Oct 11: Using a risk-based approach to comply with FDA's 21 CFR Part 11
Register Now
About
Ketryx
Company
Why Ketryx
Careers
Learn
Resources
Articles
White Papers
Webinars
Product
What is Ketryx?
Connected Lifecycle Management platform for regulated medical applications
Read more
By Function
QA / RA
Dev / R&D
By Application
SaMD
GxP
Capabilities
SBOM
Integrations
Jira
By Stage
Enterprise
Startup
Pricing
Get started
Watch Demo
Log In
Log In
Watch Demo
Get Started
Blog
\
FDA
Explore tags
Compliance
FDA
Generative AI
News
Product Development
Quality
Regulatory
Risk Management
Traceability
Update
Validation
Regulations
Clinical Trial Computerized Systems Regulation Review
Jake Stowe
•
September 5, 2023
Traceability
The Ultimate Guide to Requirements Traceability Matrix (RTM)
Erez Kaminski
•
August 30, 2023
Regulations
The FDA drops a Cybersecurity Compliance SBOM in 2023
Erez Kaminski
•
September 21, 2023
Regulations
The Turtle Problem
Jake Stowe
•
August 30, 2023
Regulations
Why the FDA’s Most Common Warning Letter Might Surprise You
Erez Kaminski
•
August 30, 2023
Regulations
Key Takeaways from the first Safety-critical Software Meetup in Boston
Erez Kaminski
•
August 30, 2023
Traceability
A brief overview of cloud security for standard and safety-critical software
John Koontz
•
August 30, 2023
Discover a new way to develop
regulated software
Creating and managing the lifecycle of a medical application is expensive, time-consuming, and error-prone. But what if it didn't need to be?
