Newsletter | January 17, 2025

01.17.25 -- AI's Potential Must Reconcile With R&D And Regulatory Bottlenecks

SPONSOR

Webinar: Can We Enable Clinical Trial Operations Without Human-In-The-Loop?

To drive forward the promising pipeline of breakthrough therapies while curbing costs, industry futurists are putting their bets on technological advancements and GenAI to reshape the drug development life cycle. This session is an invitation to rethink traditional approaches, consider innovative risk mitigation strategies, and envision a future where clinical trials are faster and more efficient but also potentially free from human limitations. Register here.

CLINICAL DATA MANAGEMENT & ANALYTICS

AI's Potential Must Reconcile With R&D And Regulatory Bottlenecks

Evaluate's Daniel Chancellor explains that by working together to expand AI resources and adapt regulatory frameworks, the FDA and others can ensure the benefits of AI are fully realized while maintaining high standards of safety and efficacy.

Deconstructing Central Rating In Clinical Trials

What is central rating, and how can it improve data quality and success rates in clinical trials?

Harness AI Beyond Chatbots to Innovate Medical Information Offerings

Take an in-depth look and the challenges and benefits of incorporating AI solutions to enhance Medical Information (MI) services and the necessity of regulatory compliance.

Real Solutions To Simplify The Digital Data Flow

An efficient flow of complex data is critical for timely, informed decision-making during clinical trials. Explore four key strategies to simplify your digital data flow.

Introduction To An End-To-End Clinical Data Science Platform

Watch to learn about an end-to-end clinical data science platform designed to streamline the rapid generation of deep insights from clinical trial data, enabling efficient delivery of crucial analyses.

TRIAL MONITORING

Using Critical To Quality (CtQ) Factors To Identify The Critical Data For RBQM

Based on ICH E8(R1) quality by design (QbD) principles, experts explain the use of critical to quality (CtQ) factors to identify critical data that focuses the end-to-end RBQM process on patient safety and trial results.

The Critical Role Of The Medical Monitor

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

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  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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