Newsletter | August 9, 2024

08.09.24 -- The Power Of Data Sharing: Revolutionizing Site Performance In Clinical Studies

CLINICAL DATA MANAGEMENT & ANALYTICS

Ensuring Data Integrity With Third-Party Labs To Avoid Submission Pitfalls

The FDA recently announced that they have seen an increase in the number of entities that contract out testing or services where the data provided by said firms was fabricated, duplicated, or just deemed “unreliable.” Here's what you can do.

How Standardizing Data Collection Enables Scalability In Clinical Trials

In an era of tightening capital and heightened regulatory scrutiny, standardizing data collection in clinical trials emerges as a pivotal strategy for efficiency and scalability.

Optimizing Clinical Supply Chain With Advanced Technology

IQVIA Technologies' Vice President and General Manager of IRT Kevin Landells and Senior Director of Product Management of IRT Stefan Dürr delve into real-world examples and practical AI applications.

Subjective Measures, Objective Outcomes: Data Quality In AD Trials

This post explores key measurement tools in Atopic Dermatitis (AD) clinical trials, specifically EASI and Total BSA, highlighting the importance of accurate measurement and strategies to improve data quality.

How Optina Diagnostics Used EDC In Earlier Disease Detection

Understand how Optina Diagnostics streamlined operations and achieved significant milestones by leveraging Castor's tools in its effort to revolutionize the diagnostic process for Alzheimer’s.

Walking Studies: Transforming Medicine With Patient Precision, Privacy

Discover how advancements in personalized medicine and innovative trial approaches are reshaping the future of healthcare, offering unparalleled insights into individual health journeys.

AI Without The Hype: Realizing High-Value Business Transformations

Read this high-level summary to better understand how artificial intelligence can improve product quality, accelerate decision-making, reduce operational costs, and enable preventive maintenance services.

TRIAL MONITORING

The Power Of Data Sharing: Revolutionizing Site Performance In Clinical Studies

Cerdi Beltré believes it’s possible to develop a global and objective way to measure investigator site performance for metrics such as startup duration, screen-pass rates, or rate of enrollment. It just won’t be easy … or make some sites happy. 

The Power And Potential Of RBM In Clinical Trials

Risk-based monitoring increases overall trial oversight by balancing “must-do” data collection and “nice-to-have” data against site and patient burden — and, more importantly, patient safety.

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You're receiving the Friday edition of the Clinical Leader newsletter, focusing on Clinical Data Management & Analytics and Trial Monitoring. To make changes to your newsletter selections, update your topic preferences.

  • 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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