The Future of Documents

Update on national pilot study for pharmaceutical companies creating ePI

In 2022, the Swedish Medical Products Agency (Swedish MPA) selected Fonto as the editor of choice for the creation of electronic structured SmPC’s. Over the past few months, the Swedish MPA has developed an XML template adapted for Fonto. Electronic product information In a Proof-of-Concept model, information elements are divided into categories depending on the

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Fonto 8.3: Say hello to a more powerful Fonto

When viewing content changes made over time in Fonto Document History, the ability to see changes made to the entire publication has been on both our and many clients’ wishlist for a long time. We’re proud to announce that, after working tediously on it for the past releases, we have created exactly that. Publication mode.

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Research results have been published in the International Journal of Research Publications

To create the most user-friendly online XML editor, we do a lot of research. User experience interviews, but also research on futuristic features and technical challenges. This research is done by our engineers, but also supported by talented students from the Delft Technical University and The Hague University of Applied Sciences. Online collaboration Great documents

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Fonto 8.2 is out right now

As the days once again grow shorter and darker, it is time for another release of Fonto. For this release, we maintained the focus on making improvements instead of adding new features. This doesn’t mean there aren’t any new things to find, you will notice some of the outline is now sticky when scrolling, and

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The Future of Standards: the ISO Annual Meeting 2022

We are present at ISO’s Annual Meeting, a meeting for all standards developing bodies worldwide. For the first time this year, the event is open to other organizations and companies that work with standards developing bodies. Against the spectacular backdrop of downtown Abu Dhabi, four full days of meetings, discussions and networking events are taking

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Structured content for pharma

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

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Global Pharmaceutical Regulatory Affairs Summit: Structured Content and Integrated Data

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

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