Business Best Practices for Running a Clinical Research Site
Discover how eSource platforms revolutionize clinical trials by simplifying data collection and ensuring accuracy, accessibility, and reliability.
Education
How Your Study’s Informed Consent Can Help Simplify Study Startup
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Simple Ways to Uncover Research Compliance Blind Spots
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
The Importance of a Large Network of KOLs for DMCs
In the complex landscape of clinical trials, the data monitoring committee (DMC) serves as the cornerstone at the intersection of
2024 Site-Sponsor-CRO Collaboration Survey Report
The Site-Sponsor-CRO Collaboration Survey Report highlights challenges in collaboration, offering actionable insights from 200+ professionals to improve trials.
Revised Common Rule Reference Guide
The revised Common Rule introduces new exemptions, refined consent elements, and alters IRB oversight for multisite and minimal-risk research.
Clinical Data Management
SITE TECHNOLOGY Clinical Data Management Streamline Your Data Collection and Management Standardize your clinical data practices to accelerate collection, ensure
Empowering Clinical Trials: The Pivotal Role of eSource
Discover how eSource platforms revolutionize clinical trials by simplifying data collection and ensuring accuracy, accessibility, and reliability.
Adapting to the Evolving Era of Oncology: Implications and Strategies for Research Institutions
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Building Buy-in: Strategic Training for Clinical Research Success
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Clinical Trial Management System (CTMS)
Site Technology CTMS Clinical Trial Management System (CTMS) A CTMS is responsible for managing all operational aspects of a clinical
From Simulation to Success: Stress Testing Your Inspection Readiness
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.