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.
Education
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.
Reviews FAQ
REVIEWS Frequently Asked Questions Find answers to our most frequently asked ethical review questions here. Can’t find what you need?
Decentralized Clinical Trials Involving Biologics: Unique Challenges
Join this webinar to learn about FDA insights on DCTs and biologics. Dr. Eisenman discusses biosafety, risks, and key considerations for safe trials.
Medicare Coverage Analysis in Oncology Trials
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.
Preparing Your Action Plan for the FDA sIRB Mandate
Navigating research compliance often means addressing unseen challenges. Explore strategies to identify blind spots and strengthen oversight frameworks.