# CircleCI in Regulated Software Development **URL:** \ **Category:** Community Projects\ **Created:** [July 2, 2017, 4:19pm UTC](https://discuss.circleci.com/t/circleci-in-regulated-software-development/13914 "2017-07-02T16:19:03Z")\ **Posts on this page:** 3\ **Page:** 1
**Author:** ![wtriplett](https://avatars.discourse-cdn.com/v4/letter/w/e95f7d/32.png) [@wtriplett](https://discuss.circleci.com/u/wtriplett)\ **Post date:** [July 2, 2017, 4:19pm UTC](https://discuss.circleci.com/t/circleci-in-regulated-software-development/13914/1 "2017-07-02T16:19:03Z")
Hi, We are an academic research lab working to transition a software product to clinical use. It requires FDA-style software validation, and we’re wondering if anyone else in a similar situation is using CircleCI’s testing framework to simplify the testing. Would love to share experiences, and perhaps collaborate on a white-paper if anyone is interested. Best, -WT ---
**Author:** ![ndintenfass](https://sea2.discourse-cdn.com/circleci/user_avatar/discuss.circleci.com/ndintenfass/32/156_2.png) [@ndintenfass](https://discuss.circleci.com/u/ndintenfass)\ **Post date:** [July 14, 2017, 6:48am UTC](https://discuss.circleci.com/t/circleci-in-regulated-software-development/13914/2 "2017-07-14T06:48:49Z")
We are working on some new features designed to allow centralized control of sensitive resources, particularly for giving more options to control changes to production systems. Would love to hear more about your requirements and see if some of our upcoming plans will meet the needs of your regulatory obligations. ---
**Author:** ![system](https://global.discourse-cdn.com/circleci/original/3X/5/1/511608acda8e85906e15909b57bd0a46c1dbe291.png) [@system](https://discuss.circleci.com/u/system)\ **Post date:** [June 18, 2018, 11:41am UTC](https://discuss.circleci.com/t/circleci-in-regulated-software-development/13914/3 "2018-06-18T11:41:55Z")