How to Reduce Compliance Risk in Packaging & Labeling
There is no such thing as a small print error on pharmaceutical drug labels or packaging. One missing dot or dash can be harmful to consumers and result in substantial recall costs for your company.
Inadequate manual inspection processes are to blame for print errors, these labor intensive proofreading marathons are only as foolproof as humans themselves. Manual inspections are also concerning for a lesser known reason – they may not comply with the new data-integrity standards.
This whitepaper discusses how automated inspection will outperform manual processes on every key measure, and how implementing a quality control solution will help you meet the new regulatory standard for data integrity.
Download your copy of our whitepaper.