Connect with WCG at Research Revolution
Discover innovative, next-generation solutions for research sites — designed to accelerate study activation, optimize operational efficiency, and digitally transform ethical oversight in clinical trials.
Visit our booth or schedule a meeting to learn how WCG is redefining site enablement, IRB review, and beyond. Explore streamlined, evidence-based solutions that empower research sites to operate more efficiently, reduce administrative burden, and deliver safer, faster, high-quality clinical trials.
Why Partner with WCG Clinical?
- Optimize Every Phase: Our comprehensive enablement approach streamlines study start-up, simplifies administration, and drives measurable performance improvements for research sites — so you can focus on what matters most: patient outcomes and research quality.
- Proven Impact: Last year alone, WCG completed over 8,000 site coverage analyses, budgets, contracts, and CTMS builds — all with turnaround times of less than five days for coverage analysis, budget development, contract review, and CTMS build services.
- Simplify IRB Review: Experience WCG’s ClinSphere™ eReview Manager, which offers unmatched speed, transparency, and regulatory excellence, giving research sites and study teams confidence in every aspect of the ethical review process.
Visit us at WCG’s booth or contact us in advance to schedule a meeting during the conference.
Meet WCG
Tuesday, Oct. 28, 10:55 a.m. – 11:30 a.m.
Innovation Showcase
Revolutionizing Ethical Oversight: The Future of IRB Management in a Digitally Connected Research World
As clinical research grows in complexity and velocity, the demand for efficient, transparent, and ethically sound review processes has never been greater. In this session, WCG will explore how centralized IRB oversight is evolving in the era of digital transformation, with a special focus on integration with eISF platforms, like Florence.
Drawing from real-world experience, this talk will dive into how WCG’s new ClinSphere™ eReview Manager accelerates study start-up, reduces administrative burden, and enhances regulatory compliance, without compromising participant safety. Attendees will gain insights into the shifting expectations around IRB coordination, the role of digital tools in streamlining submissions and approvals, and how sites and study teams can future-proof their ethical review infrastructure.
Presenter:
Tuesday, Oct. 28, 11:30 a.m.-12:15 p.m.
Reimagining Site Feasibility: Data-Driven Partnerships Between Sites and Sponsors
The traditional approach to site feasibility often falls short — burdening sites with repetitive questionnaires and yielding limited predictive value for sponsors. This panel brings together experts from research sites, sponsors, and technology innovators to explore how data, digital tools, and collaborative models can reshape feasibility assessments. We’ll discuss real-world strategies for streamlining the process, improving site selection accuracy, and enabling earlier, more transparent engagement between stakeholders.
