News & Insights
Leveraging Local Expertise
Efficiently negotiating and finalizing Clinical Trial Agreements (CTAs) is a cornerstone of successful clinical trial management in Europe. While the EU Clinical Trials Regulation (CTR) seeks to create a
Improving Clinical Trials Through Better Planning and Communication
Recently, I attended a conference where I had the opportunity to connect with numerous professionals involved in clinical trials, including individuals from pharmaceutical companies, consulting firms, and contract research
Five Things to Consider When Negotiating Contracts for Real-World Evidence Studies
Real-World Evidence (RWE) studies are a type of research that utilizes real-world data (RWD) to evaluate the safety, effectiveness, and outcomes of medical products in real-world settings. RWD
Delays in Site Start-up – Prevention Is the Key to Making a Difference
In Part 3 of this study start-up series exploring reasons for Site activation delays, ICE Global Consulting’s Head of Site Readiness, Maria P. Ladd, digs into the complexities
Delays in Site Start-up = Delays in Study Results
In Part 2 of our study start-up series, ICE Global Consulting’s Head of Site Readiness, Maria P. Ladd, explores how factors across the various study teams can lead to
Delays in Site Start-up, the Perpetual Cycle
In a multipart series, ICE Global Consulting’s Head of Site Readiness, Maria P. Ladd, explores factors leading to Site Start-up delays. Part 1: Factors for Delays During