Jim ButschliHomeSystech Announces Program for Rapid DSCSA ComplianceNinety-day compliance program enables U.S. pharmaceutical companies that distribute prescription drugs within the U.S. to meet November 2017 DSCSA deadline.January 26, 2017HomeBest Practices for Global Commercial Supply in an Evolving MarketPCI’s Feb. 9 serialization seminar to focus on establishing and developing serialization regulations that vary from country to country.January 26, 2017HomeBest Practices for Global Commercial Supply in an Evolving MarketPCI’s Feb. 9 serialization seminar to focus on establishing and developing serialization regulations that vary from country to country.January 26, 2017MaterialsBest Practices for Global Commercial Supply in an Evolving MarketPCI’s Feb. 9 serialization seminar to focus on establishing and developing serialization regulations that vary from country to country.January 26, 2017HomeVetter Starts Center for Visual Inspection and LogisticsCDMO’s Expanded Ravensburg Vetter West site provides increased capacity for quality control, cold and room temperature storage of pharmaceuticals as well as enhanced warehouse, logistics and supply chain functions.January 25, 2017InspectionVetter Starts Center for Visual Inspection and LogisticsCDMO’s Expanded Ravensburg Vetter West site provides increased capacity for quality control, cold and room temperature storage of pharmaceuticals as well as enhanced warehouse, logistics and supply chain functions.January 25, 2017MaterialsNutraceuticals Help Capsule Filler Market GrowConsumption of nutraceutical capsules as part of healthier lifestyle efforts is helping to trigger the global capsule market, with one firm predicting Compound Annual Growth Rate of 4.9% by 2024 for the market.January 24, 2017MaterialsFDA Issues Regs on Combination ProductsExplains final rule on CGMP requirements for combination products for which the agency issued a draft document in Jan. 2015. No new requirements were established. Postmarketing safety report final rule also provided.January 23, 2017Medical Device/PackagingFDA Announces Draft Guidances on Medical Product CommunicationsGuidances provide agency recommendations on labeling, as well as unapproved uses of approved or cleared medical products. Commissioner Robert Califf, M.D., notes reopened comment period extending to April 19, 2017.January 20, 2017HomeWhat To Expect in Medication Adherence PackagingIn this Q&A, Walter Berghahn, Executive Director, Healthcare Compliance Packaging Council, discusses packaging, technology, and cost issues in the ongoing effort to improve patient adherence to medication regimens.January 18, 2017Previous PagePage 65 of 135Next PageTop StoriesMedical DevicesWhat's On the Brain of a Principal Packaging Engineer?Matt Jenkins, Principal Packaging Engineer at Stryker, reflects on the challenges and opportunities in med device packaging engineering, from current regulations to the diminishing “deep work.”Temp Control/Cold ChainThrough the Line Podcast: Digital Solutions Improve Serialization and Cold Chain ManagementPMMI NewsMeeting Sustainability Goals Requires CollaborationTemp Control/Cold ChainTeva Pharmaceuticals Proves Sea Freight Viability for Temperature-Sensitive MedicinesSponsor ContentSmarter Static Monitoring for Healthcare Packaging Lines
