WCG
Set Your Studies Up for Success From the Start
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Latest posts
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What Is a Site Initiation Visit (SIV) in Clinical Trials?
Before a single patient can enroll in a clinical trial, a critical milestone must occur: the site initiation visit. For sponsors, contract research organizations (CROs), and site teams alike, the SIV signals that a site is trained, compliant, and ready to begin. Understanding…
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Improving Trial Delivery Starts with Protocol Design
Protocol design is one of the most important drivers of clinical trial success, influencing everything from study start-up timelines and participant recruitment to site burden, protocol amendments, and overall trial efficiency. As trials become increasingly complex, sponsors and…
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Study Activation Delays: The Invisible Rework Impacting Research Sites
Study activation should be one of the more predictable parts of running a clinical trial. The protocol is finalized, the budget is negotiated, and the regulatory package is ready. Yet for many research sites, this stage is where delays quietly accumulate. Pharmacy teams pull…
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What Is a Clinical Research Organization (CRO) vs. a Clinical Trial Sponsor?
Understanding who does what in a clinical trial isn’t just a formality. It shapes how studies are structured, how responsibilities are assigned, and how regulatory accountability flows from start to finish. What Is a Clinical Trial Sponsor? According to International Council for…
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WCG IRB+ Expedites Phase I CRISPR-Edited CAR-T Cell Therapy Trial
The post WCG IRB+ Expedites Phase I CRISPR-Edited CAR-T Cell Therapy Trial appeared first on WCG .
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Seven Common Signals That Your Study May Be At Risk
Studies typically stall from multiple challenges converging at once – making it difficult for teams to accurately identify and address the root causes. Being able to recognize the core issues and deploy target solutions can be the difference between a study that hits a roadblock…
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GCP Training for Clinical Trial Sites: What You Need to Know
Good Clinical Practice (GCP) training is a regulatory requirement for all clinical trial site staff. It establishes the ethical and scientific standards investigators, coordinators, and support personnel must meet before conducting research involving human participants. GCP…
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WCG Launches Activation Intelligence to Help Research Sites Accelerate Study Start-Up and Avoid Downstream Amendments
AI-powered solution creates trusted study intelligence by identifying inconsistencies early and delivering information in the format each team needs. CARY, NC, Oct. 12, 2026 — WCG, a global leader in providing solutions that measurably improve and accelerate clinical research,…
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Investigator Meetings Explained: What Clinical Study Leads Need to Know
Investigator meetings are one of the most critical — and most misunderstood — milestones in a clinical trial. As trials become more complex, global, and data-driven, these meetings play an increasingly important role in helping sites understand the protocol, align on…
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How to Make Real-World Performance Data Work for Your Trial
Clinical trial teams have access to more data than ever before. Benchmarking databases are growing, AI models are maturing, and cross-industry insights are increasingly available to sponsors and contract research organizations (CROs). But data alone doesn’t automatically…