Newsletter | July 3, 2025

07.03.25 -- Integrating QMS And eTMF For Proactive Clinical Trial Quality

FEATURED EDITORIAL

Integrating QMS And eTMF For Proactive Clinical Trial Quality

In today’s clinical trial landscape, where complexity is the new challenge, integration is not optional: QMS defines quality, and eTMF proves it. 

INDUSTRY INSIGHTS

7 Considerations For eCOA Technology Solutions

Choosing the right vendor, solution, and deployment model is critical for a clinical trial to be successful. As a sponsor, consider these seven best practices when selecting the best eCOA.

Top 10 HEOR Trends

This report outlines ten defining HEOR trends influencing global health decision-making.

eSource Vs. EDC: Reimagining Your Clinical Trials

Explore how an eSource approach to clinical trial data can reduce site burden, eliminate double data entry, minimize queries, and enhance remote monitoring.

Unlocking Potential AI And ML In Pharmacovigilance

Artificial intelligence (AI) and machine learning (ML) hold transformative potential in pharmacovigilance (PV), with the ability to enhance the efficiency, accuracy, and timeliness of drug safety monitoring.

Waiver Of Consent vs Waiver Of Written Consent

Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.

Frequently Asked Questions About IRMS MAX

Improve your information access and capabilities with the definitive gold standard of medical information systems.

SURVEY

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