Does anyone know if Jenkins are compliant according to ISO13485 for medical device development. The way my consultants see it using 4.2.5 & 4.1.6 in ISO13485:2016 one can use risk management to validate the use of this tools for QMS systems.
Has anyone here any experience of this? -- You received this message because you are subscribed to the Google Groups "Jenkins Users" group. To unsubscribe from this group and stop receiving emails from it, send an email to jenkinsci-users+unsubscr...@googlegroups.com. To view this discussion on the web visit https://groups.google.com/d/msgid/jenkinsci-users/3744052e-5e1e-456d-b932-0fba2047cdf5%40googlegroups.com. For more options, visit https://groups.google.com/d/optout.
