GSTT-CSC / GSTT-CSC/project-template
MLOps & Medical Device Regulations compliance
- Dominant language
- Python
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Description
Do we need to have a separate repo for Medical Device Regulations compliance? Things like quality management system, requirements traceability etc. Ideally we want a single CI/CD process that is suitable not only for ML but also ML in a regulated environment. Should we do it all in this repo and split it out if it makes sense?
My sense would be let's solve the entire CI/CD pipeline here, and then split out components later.
See:
https://about.gitlab.com/solutions/iso-13485/
https://dojofive.com/2019/11/04/accelerating-medical-device-development/
https://gist.github.com/pwighton/ebc66ef6d29015a8615623d64fc3547b
https://github.com/innolitics/rdm
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