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RAPS Regulatory Intelligence Conference 2026

March 3, 2026 - March 4, 2026

https://www.raps.org/riconf/home

Hyatt Regency Baltimore

Hyatt Regency Baltimore Inner Harbor
300 Light Street, Baltimore, MD 21202

Organiser

Register today for the 2026 RAPS Regulatory Intelligence Conference, Baltimore, USA, where you can join us and learn more about regulatory intelligence activation.

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About the conference

The Intelligence You Need. The Insights You Trust.

The RAPS Regulatory Intelligence Conference enables regulatory professionals to deepen their understanding of regulatory intelligence on a global scale where they can forge connections and apply practical solutions directly within their organizations.

If you are responsible for making data-driven decisions, reducing strategic errors, and improving regulatory compliance, make plans to join like-minded professionals to discuss cutting-edge strategies and cultivate innovative thinking.

Navigating the intricate landscape of regulatory intelligence and regulatory affairs, as well as broader regulatory compliance, requires more than just knowledge; it demands foresight. In an era of rapid scientific advancements and an evolving regulatory environment, staying abreast of changes is more crucial than ever. This conference is a targeted deep dive into the most pressing regulatory intelligence (RI) and policy best practices and challenges, to arm professionals like you with the insights you need for the challenges ahead.

Come and meet Infodesk

We are attending this event as gold sponsors so come and see us at the Infodesk booth, table 4, and see regulatory intelligence activation in action. See how Infodesk turns regulatory complexity into strategic clarity with current, curated intelligence. Also see the new Regulatory Workflow Solution, which goes beyond any other solution to move your organization from regulatory update to internal action, with structure, speed, and full traceability.

Regulatory intelligence activation presentation

Observe, Interpret, Activate: Scaling Human Expertise in Regulatory Intelligence

Tuesday March 3

1:45 pm – 2:10 pm

Brett Bonner, Chief Product Officer at Infodesk will be joined by VIP Infodesk customer Barbara Bovy, Head Quality Intelligence & QMS, UCB, who will be discussing regulatory intelligence activation, specifically: “Observe, Interpret, Activate: Scaling Human Expertise in Regulatory Intelligence”.  Come to the presentation to learn more about:

  1. How you can see more value from regulatory intelligence with regulatory intelligence activation.
  2. How to act on regulatory intelligence through regulatory compliance workflows throughout RI, RA, GxP, QA and other teams involved in the regulatory ecosystem and value chain. 
  3. Real-life examples from UCB. 

Presenter profiles

Brett Bonner

Chief Product Officer, Infodesk

Brett is on mission is to solve the bottleneck between pipeline and patient with regulatory intelligence that helps scale human expertise. A Chief Product Officer who has led enterprise software companies through transformative growth, Brett believes passionately in building products that solve concrete challenges and deliver measurable value, solving customer problems with the aim of creating lasting value by unlocking new opportunities at the intersection of AI and enterprise software. Brett is the foremost industry leader delivering AI technology to do this.

Barbara Bovy, PhD

Head Quality Intelligence & QMS, UCB

Barbara Bovy has been working in regulatory, pharmacovigilance and quality for 15 years+. Since 2024, she built a new department in UCB Quality, coordinating intelligence and QMS across the company. Her background includes key diplomas such as a PhD in Pharmacovigilance and a Master in Epidemiology. She started her career in Regulatory Authorities, including EMA. She then became EU QPPV at Mithra Pharmaceuticals where she built the Pharmacovigilance QMS and was directly involved in pharmacovigilance operations, before joining UCB where she led Auditing and Compliance for GLP, GCP and GVP, being responsible for the audit strategy in those GxP and hosting corresponding regulatory inspections. She is currently engaged in different associations and workstreams to shape industry interpretation of some regulatory texts. Barbara is also on the panel of experts at the RAPS RI Conference, 2026, to discuss how quality is increasingly integrated into intelligence functions that inform regulatory, compliance, and business strategy.

See the Infodesk Regulatory Workflow Solution

The Infodesk Regulatory Workflow Solution is a brand new, purpose-built solution that helps regulatory, GxP, quality, and pharmacovigilance teams turn regulatory updates into structured, auditable actions. It streamlines impact assessments, improves collaboration, and brings clarity to complex workflows. See it in action at table 4.