×

Learn how to accelerate your medical device development.

First Name
Last Name
Company
Industry
Country
State
Province
Pending Opt-In
All fields are required. Your privacy is important to us.
Thank you!
Error - something went wrong!

TIR45 | An AGILE Approach to Software Regulatory Requirements

BeanStock Ventures brought together a panel of medical device software experts to bridge the gaps between modern software development and regulatory requirements. 

AGILE development can maintain its adaptive nature while still being complaint by following guidance provided by TIR45, a recognized consensus standard by the FDA, among other best practices. This panel de-mystifies the beliefs that Agile development lacks the proper controls for producing safe and effective software and that the regulation is burdensome. The panelists share experiences, ideas and tools used to be compliant and still be adaptive and effective.

Learn more about our partnership with BeanStock Ventures

Previous Flipbook
Jama Connect™ and FDA 21 CFR Part 11
Jama Connect™ and FDA 21 CFR Part 11

Learn how Jama Connect, the leading solution for requirements, risk, and test management helps FDA-regulate...

Next Flipbook
Velentium and Jama Partner for Improved Medical Device Development
Velentium and Jama Partner for Improved Medical Device Development

Learn how Jama Software is partnering with Velentium to support innovative medical technology companies wit...