Welcome to a digital seminar series on Preparing for Impact: Maximizing the Utilization of Research.

Published 28 August, 2025Information, Seminar

As researchers in a rapidly evolving medical landscape, translating your work from bench to real-world solutions requires not only scientific excellence but also strategic foresight.

As a KI researcher you are welcome to attend two sessions designed to guide you through key steps in preparing your research for maximum impact, with a focus on three essential pillars: Intellectual Property, Regulatory Requirements and Study Design for real world evidence.

Digital Seminar 1: 10th of September, 15.00-16.00

This time we will cover:

  • Impact support at KI

An overview of the support available to researchers who wish to create societal impact from their research-based knowledge.

  • The Horizon Europe call Pathfinder Challenges

An overview of Pathfinder Challenges, with focus on the challenge “Generative-AI based Agents to Revolutionize Medical Diagnosis and Treatment of Cancer”.

  • Safeguarding long-term value: Early engagement with intellectual property strategy

We’ll discuss the importance of early engagement with intellectual property strategy—highlighting why protecting your innovations before publication is crucial for long-term value.

No registration needed, just join this teams link

Digital Seminar 2: 2nd of October, 12.00-13.00

This time we will cover:

  • Impact support at KI

An overview of the support available to researchers who wish to create societal impact from their research-based knowledge.

  • The Regulatory Roadmap: Early alignment for future approval

We’ll touch on regulatory pathways, helping you understand how early alignment with medical device regulations can save time, reduce risks, and accelerate the journey from discovery to deployment.

  • From Evidence to Implementation: Data that bridges research and practice

We’ll explore how to design studies that are not only scientifically sound but also feasible and relevant for future clinical or commercial use. This means considering studies beyond efficacy—such as feasibility, usability, cost-effectiveness, and implementation research—to ensure your innovation is practical, adoptable, and ready for real-world settings.

No registration needed, just join this teams link