Applied Clinical Trials Magazine

Applied Clinical Trials Magazine Your Trusted Clinical Trials Management Resource

How can the industry build greater trust and awareness around clinical trials?Part two of this series features Andrelia ...
06/05/2026

How can the industry build greater trust and awareness around clinical trials?

Part two of this series features Andrelia Allen and Rebecca Johnson, PhD, of Merck discussing key considerations around representation in clinical trials and community engagement.

Watch part two in the comments šŸ‘‡

What makes social media worth your time?We want your feedback on the content, formats, and channels you find most valuab...
06/03/2026

What makes social media worth your time?

We want your feedback on the content, formats, and channels you find most valuable on social.

In just 2 minutes, you can help shape future content across our brands and gain access to our Q1 Social Intelligence Snapshot, featuring exclusive social engagement insights from the Industry Science One audience.

šŸ“ˆ Share your perspective. Help shape what's next. Take the survey: https://hubs.li/Q04jQyMQ0

Happening tomorrow! Learn how leading trial teams are modernizing eConsent without increasing compliance risk.Donā€™t miss...
06/03/2026

Happening tomorrow! Learn how leading trial teams are modernizing eConsent without increasing compliance risk.

Donā€™t miss your chance to gain actionable guidance on:
āœ” Qualified vs. nonqualified signatures
āœ” Managing mixed modality studies
āœ” Strengthening audit trails and reconsent workflows

Register now before tomorrowā€™s session begins: https://hubs.li/Q04hxC2_0

How can the industry make clinical trial information more accessible?In part one of this series, Andrelia Allen and Rebe...
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 šŸ‘‡

Still building study budgets through manual protocol review and data entry? AI-driven protocol ingestion is changing the...
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 GrantPlanā€™s AI-powered Protocol Ingestion helps teams move faster from protocol to budget by automatically extracting key study details, visit schedules, and assessments.

Youā€™ll learn:
ā€¢ How AI accelerates budget development workflows
ā€¢ Where automation can improve efficiency and reduce errors
ā€¢ Why human oversight remains essential in the budgeting process
ā€¢ Whatā€™s next for protocol ingestion technology

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

Clinical trial recruitment delays are still slowing down progress for targeted therapies but thereā€™s a better way forwar...
05/22/2026

Clinical trial recruitment delays are still slowing down progress for targeted therapies but thereā€™s a better way forward.

Join this upcoming webinar to explore a data-driven approach to identifying and reaching clinically eligible patients more efficiently. Youā€™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

Electronic signatures in global trials arenā€™t one-size-fits-allā€”and getting the ā€œlast mileā€ of consent right can directl...
05/21/2026

Electronic signatures in global trials arenā€™t one-size-fits-allā€”and getting the ā€œlast mileā€ 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:
ā€¢ When qualified vs. nonqualified e-signatures make sense
ā€¢ How to reduce complexity in mixed modality studies
ā€¢ What robust eConsent really requires beyond the signature itselfā€”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

Today we recognize Clinical Trials Day and the people across the industry working to advance clinical research.Applied C...
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 ā¬‡ļø

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

Clinical trial timelines arenā€™t slowing down, but outdated, manual study builds are holding teams back.Every delay, rewo...
05/05/2026

Clinical trial timelines arenā€™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. Donā€™t miss your chance to stay ahead: https://hubs.li/Q04cMx750

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