Why this matters:
Pharma packaging failures rarely start as obvious errors. They begin as small breakdowns—outdated dosage data, claims left unchecked, mismatched inserts, generic global templates, or placeholder barcodes that quietly make it to print. This playbook dissects the five recurring packaging red flags that regulators consistently flag, explains why they keep happening across teams and markets, and lays out the process and system controls needed to prevent approval delays, batch holds, and compliance findings.
You’ll learn how to:
Audit your current packaging workflow against five regulator-critical failure points that cause delays, holds, and rework.
Set up change-controlled artwork approvals where dosage, claims, inserts, and barcodes cannot move forward without validation and sign-off.
Move from reactive fixes to preventive compliance, using structured workflows and artwork systems that withstand audits and inspections.
