
|Events|February 14, 2023
SCRS West: Clinical Tech & Innovation Summit (6/7 - 6/8/23)
June 7-8, 2023
Scottsdale, Arizona
SCRS West will flip traditional thinking about clinical trial technology rollout, training and use, while exploring new ideas and innovations being brought to market. The site voice is critical for clinical technology, and we are excited to share experiences and ideas that will impact trial technology now and in the future.
Consider what the future of clinical research will look like and leave inspired to make changes to your current approaches. Industry leaders will share trends and best practices while identifying collaborative solutions in thought-provoking sessions. SCRS West will focus on new thinking and collaborative problem-solving to power the partnerships research needs in 2023 and beyond.
Related to this article

In a video interview prior to the 2026 DPHARM conference, Andrea Valente, CEO of uMotif, shares what she expects to be at the center of the conversation—from building trust between patients and sites to where AI may and may not have a role in that relationship.

A platform-based approach connects AI across workflows, data and governance, helping life sciences organizations move from isolated wins to real scale.

In today's ACT Brief, we examine what genuine patient voice requires beyond buzzwords, why AI's next bottleneck is system integration not models, and how regulators across three jurisdictions are formalizing patient input requirements.

The clinical research industry talks about patient-centeredness constantly but embeds it too late, too narrowly, and without clear ownership, and the cost shows up in enrollment failures, protocol deviations, and outcomes that don't reflect what patients actually care about.

In today's ACT Brief, we examine FDA's expedited pathway for first-in-human trials, why operating model design matters more than sourcing strategy, and how early readiness signals predict trial risk.

FDA Opens Applications for Expedited IND Pilot Designed to Accelerate First-in-Human Trial Timelines
The pilot pairs drug sponsors with qualified research institutions to compress the path from drug identification to first-in-human study through rolling submission review and earlier coordination of institutional review board and site activation activities.
Trending on Applied Clinical Trials Online
1
Lessons from Hundreds of Clinical Trials: AI’s Successes, Gaps, and Opportunities
2
The Execution Gap: Why Clinical Trial Infrastructure Has to Be Built Before AI Can Deliver
3
DPHARM 2026: What the Patient-Site Relationship Needs Most Right Now
4
What the Epilepsy Community Has Taught Us About Trial Feasibility
5


