Michelle MaskalyHomeFDA delays e-cigarette packaging regulationsMany states have introduced, and passed, laws to address the topic, but have expressed that it should be regulated by the FDA.August 26, 2015Medical Device/PackagingWill the medical device tax ever be repealed?After almost a year of speculation, one news organization finally nailed down a possible timetable for when it might happen.August 26, 2015RegulatoryDietary supplements recalled over toxic ingredientSample analysis by the FDA showed these products contain an undeclared drug.August 26, 2015PharmaceuticalsAustralia approves first mAb biosimilarThe government estimates that increased use of biosimilar medicines will deliver $880 million in PBS savings over the next 5 years.August 25, 2015Medical Device/PackagingMedtronic acquires medical device startupThe privately held, California company is the twelfth company from The Foundry, a medical device incubator.August 25, 2015PharmaceuticalsAbbVie wants biosimilar labeling to be modifiedThe company is again challenging the FDA's implementation of the Biologics Price Competition and Innovation Act.August 20, 2015HomeFedEx launches “one-stop” cold chain solutions in ChinaWith three temperature ranges these solutions will benefit industries that require refrigeration for their shipments, particularly the healthcare industry.August 18, 2015PharmaceuticalsMedical device recalled over concerns it could ignite and burstThe company has received two reports of incidents in which the device has malfunctioned, including one death.August 18, 2015PharmaceuticalsSecret weapon in fighting counterfeit drugs? A suitcase.A Boston University researcher has designed a suitcase-type device that can detect fake drugs.August 13, 2015PharmaceuticalsExcuse me, but is that Viagra in your herbal product?FDA alleges herbal supplement has the same active ingredient as Viagra in it.August 12, 2015Previous PagePage 18 of 39Next PageTop StoriesSupply ChainFDA Launches PreCheck to Accelerate Domestic Drug Facility ApprovalsThe two-phase program is designed to expedite the approval of new pharmaceutical manufacturing facilities in the U.S. by providing enhanced regulatory guidance and communication to manufacturers.PharmaceuticalsPharmaceutical Packaging Innovations Report Video InterviewTraceability/SerializationThrough the Line Podcast: Improving DSCSA Data Exchange AccuracyPMMI News2025 Packaging State of the Industry: U.S. Expands, Canada MaintainsSupply ChainWhy Is Supply Chain Visibility and Transparency More Critical Now Than Ever Before?
