Fonto Integrated Authoring Platform
Developed in collaboration with leading pharma companies
Accelerate your time-to-market
Fonto Integrated Authoring Platform (IAP) seamlessly combines the power of structured and componentized content with user-friendly, data-driven authoring, using AI tools in the best possible ways. Developed in collaboration with leading pharma companies, Fonto IAP is the culmination of expertise from the renowned Tridion Docs component content management system and Fonto Editor, extended with the other powerful Fonto products. Fonto IAP is your all-in-one solution for efficient, integrated, and cutting-edge content creation.
It took me about five hours to redo the authoring of this section, considering all the tables and data content which is available. In contrast to this, usually it would take me a minimum of 10 to 15 hours to complete the same work.
End-to-end integrated solution
Fonto IAP offers a complete end-to-end solution, eliminating the need for tedious custom development. Instead, the platform is primed for effortless configuration, ensuring you’re up and running in no time.
At the heart of Fonto IAP lies our robust APIs, designed for longevity and adaptability. These APIs not only promise a future-proof system but also guarantee seamless two-way integration with established systems like Veeva Vault and Documentum.
We release five new products to the market per year, and that number is growing. Per new drug application, our scientists spend 800 days on automatable work, i.e. collect, retype, change, insert and format content and data. We needed to speed up these processes and reduce the amount of costly manual work. That’s solved by Fonto IAP.
Fonto IAP case studies
Reducing time to market and costs
– Global top 5 pharma company
National pilot study for creating ePI
– Swedish Medical Products Agency
Related posts on the Fonto blog
Embracing the future of document authoring in pharma: a structured and data-driven approach
In the fast-paced world of pharmaceuticals, the clarity and precision of documentation are not just a matter of compliance, but a cornerstone of innovation and patient safety. Structured content plays a critical role in meeting the stringent regulatory…
Understanding structured content: definition and benefits
In today’s digital age, the way we manage and utilize information has evolved dramatically. Conventionally, document content is unstructured, with text, figures, and tables that authors can freely arrange in the way they want to. By structuring content,…
Read full post Understanding structured content: definition and benefits
Standardize and Harmonize Product Information with Fonto: Advancing the ePI Initiative
In the ever-evolving landscape of pharmaceutical regulations and information management, the need to standardize and harmonize product information has become increasingly crucial. At the forefront of this movement is the Swedish Medical Products Agency, Läkemedelsverket, which has recently…
Request a personalized Fonto IAP demo
Meet us at the following events
DIA Global – RSIDM
We are attending DIA Global – RSIDM in North Bethesda to discuss all structured content authoring topics in pharma. Reach out to our colleague Jan Benedictus for a discussion or demo of Fonto.
Are you attending DIA Global – RSIDM and want to meet our team? Reach out!
DIA Europe
Join us at DIA Europe to discuss everything related structured content authoring in pharma, or for a Fonto demo. Together with our RWS colleagues, we have a booth with good coffee. Looking forward to meeting you in Brussels!
Are you attending DIA Europe and want to meet our team? Reach out!
DIA Global
We are attending DIA Global in San Diego to discuss all structured content authoring topics in pharma. Reach out to our colleague Jan Benedictus for a discussion or demo of Fonto.
Are you attending DIA Global and want to meet our team? Reach out!