Newsletter | July 18, 2024

07.18.24 -- Approaches For Selecting Regulatory Information Management Vendors

FEATURED EDITORIAL

Approaches For Selecting Regulatory Information Management Vendors

Deploying a formal system for regulatory information management is a given now for all life sciences companies, irrespective of their size and focus. Regulators expect this, particularly as data rather than static documents evolves to become the default.

INDUSTRY INSIGHTS

4 Biopharmas Share Why They've Switched To Veeva Clinical Data

Learn why four top biopharmas made the switch to Vault EDC. Companies making the switch are achieving 50% faster builds and 30-50% less data cleaning effort and costs.

eCOA Design Recommendations: Applied Insights From Trial Sites, CRAs

Enhance hybrid trials with digitalization through remote data capture using smartphones, tablets, and computers, improving participant experience and data integrity.

The Impact Of Clinical Trial Payments On Site-Sponsor Relationships

The sponsor-site relationship relies on good faith, but late payments sow mistrust. Experts from BMS and CenExel Clinical Research explain how consolidating payment systems benefits both parties.

Configurability And Customization: Key Features In An eTMF Solution

Discover how a configurable and customizable eTMF can lend itself to better information control during a clinical trial while boosting security and regulatory compliance efforts.

Advancing Patient-Centric Research With DHTs

Sleep quality is pivotal for overall health. Explore how wearable digital health technologies can revolutionize our understanding of sleep and enhance research outcomes.

A Guide To RTSM For Clinical Trials

Looking ahead, the evolution of RTSM in clinical trials points towards cloud-based solutions, heightened emphasis on patient safety, and greater collaboration among stakeholders.