Managing clinical trials across disconnected systems — CTMS, CTFM, EDC, eTMF — isn't just inefficient. It's expensive.

Data silos create monitoring overruns. Compliance gaps become audit findings. And every week lost in study start-up is a week your trial falls behind schedule.

With ICH E6(R3) now in full effect, the pressure to consolidate, streamline, and modernize has never been greater. Yet most clinical ops teams are still running on point solutions that weren't built to work together and paying for it in time, budget, and risk.

This webinar is your blueprint for doing it differently.

What you'll walk away with:

Three things every clinical ops leader needs right now:

→ A clear diagnosis. Understand exactly why disconnected point solutions create operational drag and compliance exposure and what a unified CTMS approach eliminates in practice.

→ A performance playbook. See how real-time dashboards and automated workflows are helping sponsors and CROs reduce monitoring costs and compress study start-up timelines.

→ An action plan. Know precisely what ICH E6(R3) requires from your CTMS platform today and leave with a checklist to assess whether your current stack is ready.

SPEAKERS

Dinesh Kashyap Founder & CEO, Cloudbyz Dinesh has spent over two decades building clinical trial technology for global sponsors and CROs. He founded Cloudbyz on the belief that trial management deserves the same real-time visibility as any modern enterprise operation.

Vedant Srivastava Product Manager, Cloudbyz Vedant leads CTMS product strategy at Cloudbyz, with deep expertise in translating regulatory requirements, including ICH E6(R3), into platform capabilities that clinical ops teams can actually use.

Free to attend · Live Q&A included · Recording available to registered attendees