WCG

Unlock 55+ years of experience and expertise with WCG. At WCG, we are committed to evolving to meet the complexities of modern trials with cutting-edge technology, expertise, and AI-powered solutions.  Powered by the most robust clinical trial data set and AI, WCG solutions, including WCG’s ClinSphere technology platform, streamline processes and drive actionable insights at every stage of your trial Together, we can pioneer a smarter, faster way to drive research to results.  Learn more about our suite of solutions at https://lnkd.in/e-dw8TuR 

Is your site struggling with slow study start-up timelines? It's time to enlist WCG. WCG’s study start-up solutions for sites accelerate study start-up timelines by providing expert, customizable support for:  ⚙Coverage Analysis  ⚙Budget Development & Negotiation  ⚙Contract Redline & Negotiation  ⚙CTMS Study Build & Support  Improve your site’s study start-up timelines and drive research to results with WCG. Learn more at https://lnkd.in/ezj7ZXZM.   #clinicaltrials #clinicalresearch #budget #coverageanalysis #contract 

Are you looking for trusted resources to boost efficiency, enhance quality, ensure compliance, and reduce risk in your #clinicaltrials? Explore WCG’s Avoca Quality Consortium (AQC) Knowledge Center, a centralized repository of over 1,500 leading industry practices, guidelines, tools, templates, and metrics to support successful study execution. Join us for a FREE live demo and discover how joining the AQC can transform your #clinicalresearch. Register now at https://lnkd.in/edv2YS2 Avoca, A WCG Company #WCG #AQC #webinar #clinicaltrials #clinicalresearch #demo 

🚀Streamline site selection with real-time data insights from WCG ClinSphere™ Total Feasibility. Our tech-enabled solution empowers you to make informed and accurate study planning decisions. Key features include: 💻 Centralized Data Access ⚙ Configurable Processes 📊 Optimized Analytics Enhance your site feasibility processes with our self-serve application or through a high-touch, service-oriented experience. Learn more and schedule a consultation at https://lnkd.in/e9ka2SkA  #feasibility #clinicalresearch 

Is your organization prepared for the ICH E6(R3) guideline, effective in the EU as of July 23? Find out with WCG's ICH E6(R3) Readiness Assessment! Upon completion, you will immediately receive a report on your overall readiness and actionable insights across seven areas of focus. Take it for FREE now at https://lnkd.in/eTSRvWkm #regulatory #clinicalresearch #ICHE6R3

📣 Calling all #clinicalresearch site professionals! 🎤 We want to hear from YOU! The 2025 Site Challenges Survey is NOW LIVE! Share your insights on the top challenges facing sites. Your site’s participation will help shape a comprehensive industry report and drive improvements for site success across clinical research.  ⭐⭐⭐ The survey only takes FIVE minutes! Participate now at https://lnkd.in/g7zaxzbv #clinicalresearch #clinicaltrials #survey 

#DidYouKnow Although the U.S. leads in clinical trial participation overall, WHO data show that multi-regional trials, especially in oncology, rarely include a large proportion of U.S. participants. In our latest blog, Cristin MacDonald, PhD examines the growing pressure from U.S. regulatory agencies for stronger U.S. enrollment in pivotal clinical trials. Discussing recent FDA actions and guidelines, the importance of U.S. site selection, and how sponsors can adapt to this new reality to protect their development programs and patient access to novel therapies. Read now at https://lnkd.in/eXfMyuc6 #clinicalresearch #oncology #oncologyresearch #regulatory 

Get your most asked Data Monitoring Committee (DMC) questions answered with WCG's on-demand webinar! ❓What are the ideal qualifications of members who serve on a DMC? How are members selected?  Jonathan S. explains that ensuring participant safety is the core function of a DMC and requires a team with diverse skills.  Gain a better understanding of the evolving role of DMCs with our FREE on-demand webinar! https://lnkd.in/ecAA5ZGu  #DMC #DataMonitoringCommitee 

❓How much of an impact do industry professionals think ICH E6(R3) will have on clinical trial design and operations?  💡Find out with the 2025 Avoca State of the Industry Report! This report dives into responses from over 250 sites, sponsors, and providers to better understand actions toward adoption of ICH E6(R3) and its impact on clinical trial design and execution. Download the FREE report now at https://lnkd.in/eAyTMCRP Avoca, A WCG Company #compliance #ICHE6R3 

The ICH E6(R3) guideline is now effective in the EU.  🔓Unlock practical steps to assess and improve compliance at your organization with WCG's on-demand webinar. Industry experts Karen Harvey and Michelle Webb share insights from the 2025 Avoca State of the Industry Report to explore how the industry is adapting, where gaps remain, and what best practices are emerging. Elevate success for your global clinical trials and access the FREE webinar now at https://lnkd.in/ee6auJqX. #clinicalresearch #clinicaltrials #compliance #regulatory #ICHE6R3