01.16.26 -- Site Management And Oversight Become Must-Haves For Success

Medical Monitors interact with nearly all functional roles on a study team, and more experienced monitors often support and mentor less-experienced colleagues.

A connected clinical ecosystem improves participant engagement. Integrating remote monitoring and digital tools ensures more diverse participation, higher data integrity, and more efficient timelines.

Discover how Sarah Wilson, Director at Alkermes, revolutionized document collaboration using a document review platform to boost efficiency and overcome regulatory challenges in medical writing.

Trial success depends on more than technology alone. Addressing human factors like rater drift and training is essential to prevent data loss and ensure reliable neurological assessment outcomes.

Clinical teams can overcome data access and analysis challenges with real-time workflows, traceable decisions, and flexible analytics to accelerate insights and improve collaboration.

Explore an innovative approach to seamless, real-time data capture through wearable sensors that aligns with the FDA's efforts to modernize trials through Digital Health Technologies (DHTs).

By aligning biometrics expertise with advanced technologies and global regulatory standards, sponsors can optimize resources, ensure patient safety, and bring transformative therapies to market faster.

Learn how AI solves repetitive, time-intensive manual tasks to decrease time to First Patient In (FPI) for digital and decentralized clinical trials, dramatically accelerating study startup.

Explore a solution for early-stage life sciences organizations featuring dimensional charts of accounts, program and project management, multi-subsidiary support, and mass securities.