Different owners need different evidence views.
Good AI PracticeAI product owner
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
data science lead
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
clinical/scientific owner
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
QA
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
regulatory strategy
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
safety/PV owner
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
model governance reviewer
This actor needs a clear route from source interpretation to owned evidence, decision, and follow-up for Good AI Practice.
Where iFeed can help without overclaiming.
bridge workSource-to-evidence mapping
Convert source material into evidence objects, owners, gaps, and next actions.
Checklist evaluation
Review completed readiness sheets and identify unclear or unsupported claims.
Governance sprint
Create a practical two-week route for inventory, role mapping, evidence review, and update protocol.
Training/workshop
Turn source reading into role-specific literacy and operational confidence.
Current public sources for Good AI Practice.
official firstThese links are the public source anchors for this workspace. Interpretation, checklists, and future assets should point back here before being reused outside iFeed.
FDA guiding principles for Good AI Practice in drug development
2026-01-14 · FDA page for common Good AI Practice principles in drug development.
EMA and FDA common AI principles news
2026-01-14 · EU-facing publication context for the common principles.
EMA/HMA AI in medicinal product lifecycle
2024-09-30 · Broader medicinal-product lifecycle reflection layer for AI use and governance.
FDA/Health Canada/MHRA GMLP principles
2021-10-27 · Ten guiding principles for Good Machine Learning Practice for medical device development.