Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Update compliance_monitoring.md #44

Merged
merged 1 commit into from
Jul 19, 2023
Merged
Changes from all commits
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
2 changes: 2 additions & 0 deletions pages/your_tasks/compliance_monitoring.md
Original file line number Diff line number Diff line change
Expand Up @@ -39,6 +39,8 @@ By knowing their capabilities institutions can spot areas of improvement and dir
* The [FAIRplus project](https://fairplus-project.eu) with its {% tool "fair-cookbook" %} provides services, tools, and indicators necessary for the assessment or the evaluation of data against the FAIR Principles.
* {% tool "fair-evaluation-services" %} are an automated approach to evaluate FAIRness of data services.
* {% tool "fairassist-org" %} aims to collect and describe existing resources for the assessment and/or evaluation of digital objects against the FAIR principles.
* The {% tool "fair-wizard" %} utilizes FAIRification resources developed by the FAIRplus project and other platforms, suggests FAIRification materials based on the FAIRification requirements, and designs FAIRification solutions for data owners, data stewards, and other people involved in FAIRification.
* The {% tool "fairshake" %} evaluates the FAIRness of Digital Objects.
* Information Security, Data Protection, Accountability
* [21 CFR part 11](https://www.fda.gov/regulatory-information/search-fda-guidance-documents/part-11-electronic-records-electronic-signatures-scope-and-application) is a standard, which outlines criteria for electronic records in an IT system to be as valid as signed paper
records. It is widely adopted in lab information systems and applications used in clinical trials and medical research.
Expand Down