Newsletter | November 22, 2024

11.22.24 -- How Can We Improve/Simplify The Clinical Trial Digital Dataflow?

TRIAL MONITORING

How Better Data Interoperability Can Unlock Better Human Trials

Data interoperability is critical to clinical trials, ensuring systems and stakeholders work together smoothly. It’s like texting between iOS and Android—without alignment, communication falters. Bill Illis of Novartis highlights similar challenges in clinical trials, where a lack of standardized protocols leads to delays and fragmented data. In this talk, he explores how industry-wide collaboration on digital protocol standards can eliminate these roadblocks and speed up clinical research.

Inspection Readiness

Learn how your company can enable productive interactions with inspectors through Inspection Readiness (IR) gap assessments, and propel to the next phase of development.

CLINICAL DATA MANAGEMENT & ANALYTICS

How Can We Improve/Simplify The Clinical Trial Digital Dataflow?

With ICH M11 expected to be adopted by the end of 2024, this Clinical Leader Live discusses the advantages of improving and simplifying the dataflow of clinical trials but also the challenges associated with creating a connected digital dataflow, including digital health channels, that spans from protocol to data collection to CSR.

CLINICAL DATA MANAGEMENT & ANALYTICS - INDUSTRY INSIGHTS

Overcoming The Top 3 Challenges In Setting Up And Managing Clinical Trials

Navigating the intricacies of clinical trials demands adept handling of document management, regulatory compliance, and financial forecasting. Learn key strategies for overcoming these hurdles.

Safety As A Science: Analytics For Trial Safety And Pharmacovigilance

Clinical trials can expose both predicted and unexpected safety signals. Understand why surveillance must therefore look beyond expected adverse events to detect possible safety signals.

How To Seamlessly Integrate NetSuite With Power BI

Unlock the power of your NetSuite data with seamless integration to Power BI. Learn how to automate data refresh, gain real-time insights, and make informed business decisions.

Drive Automation And Efficiency In Your Interim Lock Process

Medidata Interim Lock enhances automation and efficiency in managing clinical study databases by streamlining the interim lock process.

Utilize AI To Generate SDTM And ADaM Datasets

Stop spending thousands of man-hours on SDTM, ADaM and TFL generation and accelerate the delivery of clinical discoveries to patients. Transform your biostatistics deliveries with ThoughtSphere.

Medable Studio

More than just a builder, Medable Studio offers unmatched control over study creation and launch, eliminating the common roadblocks of study startup and empowering users throughout the process.

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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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