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Why pharma teams are drowning in submissions and what to do about it – Part two

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Welcome to part two of this blog series. In the first part we’ve explored the current state of the pharma industry and how the regulatory submissions process has been impacted. We’ve looked at KPIs that sponsors and CROs can monitor to ensure regulatory submission success, and we’ve analyzed the current landscape, looking at the internal […]

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Why pharma teams are drowning in submissions and what to do about it – Part one

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Regulatory affairs (RA) teams are under pressure more than ever before. Faced with a growing demand for pharmaceuticals, cumulative legislative changes and an approaching steep patent cliff, sponsors are struggling to find new ways to modernize, innovate and deliver therapeutics to market faster.   The greatest challenge isn’t just the volume of work, but the unpredictable

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Fonto Why & How: How do I set up Global vs. Local Fonto Development Tools installations

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Working with multiple Fonto Editor instances and multiple Fonto Development Tools (FDT) installations? In this blog post, we explain how to manage each editor with its own SDK version and matching tools setup. When a developer works on a single instance of Fonto Editor, it’s just one editor running on a specific SDK version. However,

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Maarten van Vulpen presenting at the Innovation stage at the Frankfurter Buchmesse 2025

Structured content and AI: get your publications out better and faster

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Last Thursday at the Frankfurter Buchmesse, Maarten van Vulpen presented on the Innovation Stage about how structured content and AI together can transform the way publishers create, manage, and distribute content. This well-received talk built on last year’s presentation, Feeding AI Models with Structured Content: The Power of XML ,but this time went further, showing

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From Word to the web: How IEC authors are embracing Online Standards Development

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Since early this year, the International Electrotechnical Commission (IEC) has been using its new Online Standards Development (OSD) platform, a fully web-based environment for drafting and reviewing international standards. Built around structured content authoring, OSD integrates Fonto as its core XML editor, enabling technical experts from around the world to collaborate on standards in a

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Fonto receives Excellence Partner Award from Ebcont

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We are proud to announce that Fonto has been awarded the Excellence Partner Award by Ebcont. This recognition underlines the strength of our collaboration and the trust we’ve built working together on multiple global projects. It’s also an encouraging sign of what lies ahead: this is just the beginning. A growing partnership Ebcont and Fonto

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How to accelerate pharma regulatory success with prepopulated templates

5 minutes of reading / / By

Pharma organizations can spend as much as $4.54B to bring a single molecule to market. The costs are only rising, while regulations are becoming more complex. This pressures organizations to manage extensive portfolios and afferent regulatory dossiers with fewer resources. When regulatory submissions take too long or are not accepted, organizations incur significant costs, from

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Fonto 8.14: More accessible, smarter, and ready for complex workflows

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With Fonto 8.14, we’re continuing to refine the editing and review experience for every user, from accessibility improvements that make Fonto easier to use with assistive technologies, to smarter APIs, more powerful metadata, and performance tuning across the board. This release is all about flexibility, control, and efficiency, helping teams handle complex content at scale

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