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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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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Moving from Word: why changing the interface is unacceptable

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 …

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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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Moving from documents to data in the Standards Publishing industry

In a very informative and recently published report by Outsell, lead analyst Tatiana Khayrullina confirms what Forrester described earlier in its ‘Future of Documents’ report:    “Despite more than 30 years of mainstream use of office authoring tools, not much has changed. Increasingly, enterprises deliver documents to customers in forms that aren’t fit for purpose. The …

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Fonto 8.0 WebinarApril 13, 6.30 pm CET / 11.30 am CST

Providing you with insights from our team and a QA session.

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