Liz TierneyTraceability/SerializationLive from Interphex: The Human Challenge in Manual AggregationSix months after the serialization enforcement date, a new challenge emerges. Staff and processes must be set up to keep rejected product… rejected.April 2, 2019HomeLive from Interphex: The Human Challenge in Manual AggregationSix months after the serialization enforcement date, a new challenge emerges. Staff and processes must be set up to keep rejected product… rejected.April 2, 2019Medical Device/PackagingLive From Pack Expo Las Vegas—RollprintFlow wrappers achieve 400 per minute with new film from Rollprint, easy-open and seal integrity.September 25, 2017HomeLive from PDA/FDA: Culture of QualityEmpowering employees with a strong sense of ownership can lead to improved outcomes and increased cost efficiency.September 12, 2017Logistics/Supply ChainPharmaceutical Cargo Thefts on the DeclineLarge-scale pharmaceutical cargo thefts descend between 2009 and 2016 as pharma and med device makers take unprecedented steps to secure their products.May 8, 2017HomePharmaceutical Cargo Thefts on the DeclineLarge-scale pharmaceutical cargo thefts descend between 2009 and 2016 as pharma and med device makers take unprecedented steps to secure their products.May 8, 2017PharmaceuticalPharmaceutical Cargo Thefts on the DeclineLarge-scale pharmaceutical cargo thefts descend between 2009 and 2016 as pharma and med device makers take unprecedented steps to secure their products.May 8, 2017HomeSwitching from 2nd Day to Overnight Shipping to Generate SavingsAt face value, overnight shipping is more costly than two-day shipping. But thanks to an analysis of the total cost, Merck was able to save money by switching to the faster shipping option for some products.October 3, 2016RegulatoryLIVE FROM PDA/FDA: An Overview of FDA’s Expectations of BiosimilarsSimilar biological medicinal products are not the same as small-molecule generics in terms of their complexity or the approval process, which evaluates residual uncertainty at each step.September 14, 2016HomeLIVE FROM PDA/FDA: Compliance to Quality: Part 1CDER’s Office of Pharmaceutical Quality aims to establish a collaborative approach with manufacturers to encourage innovation and the adoption of new technologies.September 14, 2016Page 1 of 3Next PageTop StoriesPackaging/Filling7 Success Attributes for a Super-Orphaned Drug Manufacturing SuiteTakeda manufactures one batch of infant botulism treatment every five years. Source plasma only comes from around 30 donors. Hear about their “batch right, first time” approach, because there is no second chance to get it right.Packaging/FillingPharma Manufacturers Need Agile Training Amid Employee TurnoverPackaging/FillingPharmaceutical Drones Prevent Defects in Filling/AssemblyPMMI NewsPACK EXPO East Continues Growth Trajectory With Largest Show to DateAutomation/RoboticsRange of Collaborative Palletizers Feature Integrated Stretch Wrapping