
News|Articles|April 9, 2024
Developing a Method to Learn Capper Settings to Handle Component Variations
Author(s)Genesis Packaging Technologies
One of the causes of crimp variation that can lead to integrity failures due to poorly sealed vials has been reported to be component dimensional variation. Critical dimensions of the components of a vial system (vial, stopper, and cap) can vary within manufacturing tolerances, but these ranges of variation may require adjustments to the capper settings to ensure a proper package seal.
Newsletter
Get the essential updates shaping the future of pharma manufacturing and compliance—subscribe today to Pharmaceutical Technology and never miss a breakthrough.
Trending on Pharmaceutical Technology
1
Rare Disease Treatments: Navigating the Economics of Global Innovation
2
WEF Welcomes ACG Shirwal as First Pharma Packaging Site in Global Lighthouse Network
3
Women in STEM: Early Phase Drug Development
4
Drug Digest: Outsourcing Partnerships Fuel Global Biopharma Discovery and Scale-Up
5