News & Insights
What Is a CRADA?
For sponsors and CROs exploring new sites for clinical research, Veterans Affairs (VA) hospitals are often overlooked—but they shouldn’t be. VA sites offer access to well-established infrastructure, highly experienced investigators,
Site Payments Frustrations
Ask almost any clinical trial site or sponsor to name a major pain point in study operations, and you’ll likely hear the same answer: site payments. Despite all the
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 harmonized
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 organizations
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 is data
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 of the