Hurra! Fonto has been selected as the XML editor of choice by the Swedish Medical Products Agency (Swedish MPA) for a national pilot study for pharmaceutical companies creating ePI. Electronic Product Information (ePI) ePI refers to the authorized, statutory product information for medicines (including the Summary of Product Characteristics, Package leaflet and labelling) adapted for …
It takes pharma companies about five times longer to create content, compared to other industries. Delayed drug approvals turn into an average loss of $1 million dollars per day for pharma companies. Val Swisher and Regina Lynn Preciado from Content Rules recently published an interesting e-book: “Structured Content for Pharma – Making the Case for …
In pharma—and many other industries, too—Microsoft Word is the tool to create content. It’s the natural environment for many subject-matter experts to write, edit and review content. Every author is familiar with the Word interface. But it’s not structured content that’s created … “We cannot change the authoring experience” Forcing subject-matter experts, for example medical …
Moving from Word: why changing the interface is unacceptable Read More »
Today, Jan Benedictus presented at the Global Pharmaceutical Regulatory Affairs Summit 2022 in Berlin: “The Future of Documents: Structured Content, Integrated Data”. Global Pharmaceutical Regulatory Affairs Summit The Global Pharmaceutical Regulatory Affairs Summit focuses on the challenges of IDMP, RIM, eSubmissions and Global Market Regulation in the pharmaceutical industry. The Future of Documents The Future …
Global Pharmaceutical Regulatory Affairs Summit: Structured Content and Integrated Data Read More »
How FontoXML helps pharmaceutical companies comply with future legislation In Pharma and Life Sciences structured content, or rather structured data, is a hot topic. Most, if not all companies in this industry are in the process of undertaking a multi-year cross-functional program to enable sustainable compliance with the upcoming IDMP requirements and to improve regulatory …
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