Applied Clinical Trials Magazine

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Applied Clinical Trials Magazine

Your Trusted Clinical Trials Management Resource

05/29/2026

How can the industry make clinical trial information more accessible?

In part one of this series, Andrelia Allen and Rebecca Johnson, PhD, of Merck discuss representation in clinical trial ex*****on and the importance of making clinical trial information more accessible and familiar to communities.

Watch part one in the comments 👇

05/26/2026

Still building study budgets through manual protocol review and data entry? AI-driven protocol ingestion is changing the process.

Join IQVIA to see how CTFS GrantPlan’s AI-powered Protocol Ingestion helps teams move faster from protocol to budget by automatically extracting key study details, visit schedules, and assessments.

You’ll learn:
• How AI accelerates budget development workflows
• Where automation can improve efficiency and reduce errors
• Why human oversight remains essential in the budgeting process
• What’s next for protocol ingestion technology

Register now: https://hubs.li/Q04hxV510

05/22/2026

Clinical trial recruitment delays are still slowing down progress for targeted therapies but there’s a better way forward.

Join this upcoming webinar to explore a data-driven approach to identifying and reaching clinically eligible patients more efficiently. You’ll see how different recruitment methods compare on cost, precision, and patient access and why a targeted strategy can significantly improve timelines and outcomes.

With the session approaching soon, now is the time to secure your spot and see how Quest can strengthen your recruitment mix.

Save your spot: https://hubs.li/Q04fZ37m0

05/21/2026

Electronic signatures in global trials aren’t one-size-fits-all—and getting the “last mile” of consent right can directly impact compliance, operational efficiency, and inspection readiness.

Join IQVIA experts Sonia Fischer, MHA, MBA, and Dana Liu, MBA, as they break down:
• When qualified vs. nonqualified e-signatures make sense
• How to reduce complexity in mixed modality studies
• What robust eConsent really requires beyond the signature itself—from authentication to audit trails and reconsent workflows

If your team is scaling global studies, this session delivers a practical framework you can apply immediately.

Register Now: https://hubs.li/Q04hxzTG0

05/20/2026

Today we recognize Clinical Trials Day and the people across the industry working to advance clinical research.

Applied Clinical Trials is highlighting perspectives on R&D success and reflections on what Clinical Trials Day means throughout the clinical research community.

Read more in the comments below ⬇️

05/12/2026

Clinical trial recruitment remains one of the biggest barriers to speed and success in bringing targeted therapies to market.

This webinar breaks down a smarter, data-driven approach to patient identification and outreach, showing how to improve precision, reduce cost, and accelerate timelines.

Discover why a targeted recruitment strategy with Quest can make the difference.

Save your spot: https://hubs.li/Q04fZv1K0

05/05/2026

Clinical trial timelines aren’t slowing down, but outdated, manual study builds are holding teams back.

Every delay, rework cycle, and inconsistency puts pressure on compliance and study readiness. Teams that fail to adapt risk falling behind as AI-driven workflows set a new standard.

Join this webinar to learn how to eliminate bottlenecks, reduce rework, and shift to a more strategic, future-ready approach to data management.

Spots are limited. Don’t miss your chance to stay ahead: https://hubs.li/Q04cMx750

05/04/2026

Happening this week: oncology evidence is evolving fast and real-world data is at the center of the conversation.

Join this live virtual event to hear experts discuss how RWD is being used alongside clinical trials to guide research, trial planning, regulatory strategy, and post-approval insights.

Save your seat now: https://hubs.li/Q049JNJy0

04/29/2026

If outdated, static COA libraries have been slowing your study planning and decision-making, this is for you.

Join a session presented by IQVIA to learn how to overcome it with proven strategies from industry experts Anthony Mikulaschek and Luis Gaspar.

Register here: https://hubs.li/Q049zPFf0

04/27/2026

From Journey to Action: Using Longitudinal Patient-Level Insights to De-Risk and Accelerate Clinical Trials

In this interview, Skye Hodson, PhD, of Citeline explains how longitudinal, patient-level insights across the full care journey are helping sponsors overcome enrollment delays, investigator scarcity, and protocol complexity—transforming strategy into ex*****on-ready deliverables that optimize feasibility, site selection, and measurable recruitment outcomes.

Watch Now: https://hubs.li/Q047qmJW0

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