Newsletter | May 23, 2025

05.23.25 -- The Evolving Landscape Of Data Integrity In Good Clinical Practice

SPONSOR

Webinar: How Sponsors can leverage site technology to standardize quality and improve site performance

With Central eSource, sponsors define a standard electronic source template, pre-map it to the eCRF, and send it to sites, where it can be configured locally to reflect their SOPs. Learn how sponsors can leverage the electronic source trend to accelerate site startup, standardize data quality at the point of capture, accelerate EDC entry, and enable true centralized remote monitoring.

CLINICAL DATA MANAGEMENT & ANALYTICS

The Evolving Landscape Of Data Integrity In Good Clinical Practice

Guest Column | By Andy O’Connor, ERA Sciences

ERA Sciences Andy O'Connor explores the growing focus on data integrity in GCP and how regulatory guidance is evolving to support a risk-based, system-life cycle approach.

Key AI Trial Insights From Regulators And Consultants

White Paper | Medable

AI’s transformative impact promises more efficient, cost-effective, and successful clinical trials across the pharmaceutical landscape.

How To Facilitate Good Clinical Data Review In Your Clinical Trial

White Paper | Revvity Signals Software, Inc.

Learn how to create a system based on connectivity and automation, aggregated and usable data, flexible analysis, and methods of collaborative data review by centralizing analysis and communications.

Here To Help You Succeed

Video | IQVIA Biotech

IQVIA Biotech is a standalone business of IQVIA with dedicated teams delivering clinical development solutions for biotech and emerging biopharma customers. Discover why IQVIA Biotech is the CRO partner of choice for biotech companies around the world.

Get Full-Service Support With This Biometrics Solutions Package

Brochure | Palleos

Experience a seamless and professional approach to managing clinical trials. Click here to get high-quality Biostatistics and Clinical Data Management services from a leading Eastern European CRO.

TRIAL MONITORING

Financials Of Clinical Research Still A Deterrent To PIs

Video | By Clinical Leader Live

According to Jimmy Bechtel of SCRS, part of the one-and-done PI problem is the financials associated with clinical research.

RBQM: The Connective Tissue For Data Quality

Article | Medidata, a Dassault Systemes company

Explore the role of risk-based quality management in clinical trials and how it enhances efficiency, ensures data integrity, and mitigates risks with advanced analytics and proactive monitoring.

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