03.25.26 -- STREAM Edition: 3 Pillars Of Trustworthy AI In Clinical Trials

Here, we debate sponsor-provided source document templates, weighing regulatory guidance, compliance risks, and operational impacts for smarter clinical trial documentation decisions.

AI has great potential to enhance the efforts of your team members by accelerating data interactions. Watch this webinar and discover how AI can improve clinical trial outcomes and data management.

With consistent, repeatable system builds, sponsors get a big advantage during protocol amendments and operational changes.

Explore innovative strategies for reducing Scope 3 emissions in clinical trials. Discover sustainable solutions that uphold quality and outcomes, crucial for achieving net-zero goals in healthcare research.

In this presentation, industry experts will share real-world lessons learned from managing global early-phase oncology trials.

Selecting the right functional service provider (FSP) is a critical factor in advancing clinical research programs efficiently, and this reimagined FSP model prioritizes each client’s unique objectives.

Unlock real-time data tracking, customizable reporting, and proactive compliance monitoring with the IQVIA eCOA Sculptor Portal to enhance clinical decision-making and ensure protocol adherence.

Donna Rivera of Canal Row Advisors stresses that successful and regulator-trusted AI depends on three fundamentals: high-quality, fit-for-purpose data; transparent and explainable models; and cross-disciplinary collaboration to ensure meaningful clinical impact.