EMA: Updated Day 215 PI Annex Submission Checklist for Post-Opinion Linguistic Review
Update internal labeling workflows to align with the revised checklist; ensure submission documents meet updated formatting requirements for linguistic review.
Role
Labeling Leads convert validated safety signals into accurate product information across regions. PV Bulletin surfaces PRAC SmPC recommendations, FDA safety labeling orders, and variation category changes — with workflow impacts for label governance, medical review, and regulatory submission planning.
3 updates · Sorted by impact priority
Update internal labeling workflows to align with the revised checklist; ensure submission documents meet updated formatting requirements for linguistic review.
Stakeholders, including those involved in labeling and signal management, should consider the published comments to align future processes with the regulatory expectations detailed in the draft ICH E22 guideline.
MAHs should review the updated DRGD to understand new processing timelines for variation submissions and assess how the reliance mechanism can be leveraged for faster safety updates. Adjust internal timelines and processes for post-marketing variation submissions accordingly.
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