An In-House Workshop for Sponsors and Trial Teams
Led by Eyal Wultz, Bioforum Co-founder and BionData Co-founder and President
Why This Workshop Matters
Today’s clinical trials collect millions of data points from a growing number of sources — wearables, apps, ePROs, telemedicine, imaging, and more. This surge in volume and complexity makes it harder to ensure data is complete, traceable, and submission-ready.
At the same time, regulators are scrutinizing data integrity more closely than ever. Submissions are being delayed — or rejected — not because of bad science, but because the data wasn’t properly prepared.
This workshop helps make sure yours is.
What You’ll Learn
A live, hands-on, 3–5 hour workshop tailored for 10–15 participants from your company. We cover:
- What a submission-ready data package includes – and why it matters
- How to effectively manage your CRO — including common pitfalls to avoid
- Real-life examples and actionable insights from 20+ years of experience
Who Should Attend
Clinical operations, data management, biometrics, medical writers, or anyone involved in an upcoming regulatory submission, especially those with limited experience in preparing clinical data for submission.
Why Company-Specific?
Workshops are tailored to your team so participants can:
- Ask real questions openly
- Focus on challenges relevant to your trials
- Leave with clear, practical takeaways
About the Instructor
Eyal Wultz is Co-founder of Bioforum and BionData, with over 25 years of experience in clinical research and regulatory data strategy. He has guided dozens of sponsors through successful submissions and is known for turning complex data challenges into clear, actionable solutions.
Ready to Bring This Workshop to Your Team?
Contact Eyal Wultz at eyal.wultz@bioforumgroup.com