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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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Fonto: Why & How: How do I generate IDs in a more predictable way?!

In this weekly series, Martin describes a question that was raised by a Fonto developer, how it was resolved and why Fonto behaves like that in the first place. This week, a support question came in inquiring how they could have more control in ID generation! As usual, support question! This one read like this: We

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Fonto Why & How: Why is my operation on a locked document enabled?!

In this weekly series, Martin describes a question that was raised by a Fonto developer, how it was resolved and why Fonto behaved like that in the first place. This week, a partner sees enabled operations for a document they have no rights to edit! A support question came in: an author loaded a document

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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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Fonto 8.1 is now available

The latest release of Fonto focuses primarily on improving what was already in place. After our first major release in over four years, we decided to take a release worth of time to ensure we could further polish and optimize the work that was done previously. This includes, based on your feedback, improvements to our

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