As one might expect for highly regulated industries such as pharma and medtech, our 2017 articles on regulatory developments attracted a lot of attention, coming in as our 4th most popular topic in 2017.
Our article, "New medical device regulations could impact packaging—and not just in Europe," recapped the changing regulatory landscape around the world as explained by Thierry Wagner, DuPont’s regulatory affairs director—Europe, Middle East & Africa, in the Webcast, “Speed Up Your Compliance Process—With Help from DuPont Tyvek.” He was joined by cospeaker Nicole Kaller, application & package engineering specialist—Europe, Middle East & Africa, who detailed DuPont’s efforts to help MDMs prepare documentation for their product regulatory submissions and certifications.
Another popular regulatory story in 2017 examined FDA’s plans for pharmaceutical serialization requirements. Several suppliers working with pharma offered their perspectives in “What does FDA’s DSCSA enforcement delay really mean?”
Above image source: Shutterstock/garagestock
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