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, 2017WorkforceLive from PDA/FDA: Culture of QualityEmpowering employees with a strong sense of ownership can lead to improved outcomes and increased cost efficiency.September 12, 2017Supply 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, 2017PharmaceuticalsPharmaceutical 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 StoriesRegulatoryStudy Reveals the U.S. Pharmaceutical Firms with the Most FDA RecallsAn AI healthcare platform analyzed 13 years of FDA data to identify companies with highest recall rates and most dangerous violations.Package DesignThrough the Line: At-home Test KitsPackage DevelopmentPackaging Recycling Professionals Gathered in Person and Remotely for this Year's Packaging Recycling SummitRegulatoryBridging the Barcode Divide: Challenges in Medical Device UDI ImplementationAdherence/DeliveryImproving Self-Injection Delivery of Biologics Through Better Needle Choices
