Reducing the cost and time of clinical trials
Our clinical services help Sponsors, CROs and Sites to compress their study timelines by 33%.
Our clinical services help Sponsors, CROs and Sites to compress their study timelines by 33%.
Changes to Research Made in Response to COVID-19
Learn about the requirements for IRB review of changes in research made in response to the COVID-19 epidemic.
COVID-19 and Clinical Trial Operations Resource Center
Clinical Trials in the Era of COVID-19: Changes You Need to Make Now
Part 4 [Apr. 8]: Register Now
Part 3 [Apr. 1]: On-Demand
Part 2 [Mar. 25]: On-Demand
Part 1 [Mar. 18]: On-Demand
COVID-19 Preparedness for Health Care Institutions
Watch On-Demand
The WCG Knowledge Base™ is the industry’s largest database of site and investigator insights, benchmarks, and competitive performance data.
We bring the power of our deep relationships with over 3,000 institutions, including nearly all of the largest Academic Medical Centers.
WCG services are powered by the combination of our deep clinical expertise and advanced technologies.
acceleration in study start up
Our insights-driven site selection and feasibility services together with our site budgeting and contracting services solve common trouble spots in the start up of clinical trials, helping Sponsors and CROs compress their study timelines by 33%.
increase your enrollment rates by 50%
If your study enrollment is running behind—or you want to prevent the common pitfalls in patient recruitment—our enrollment accelerator is the right solution for your team. We deploy expert resources, tools and processes to your key sites to dramatically improve enrollment rates to meet or exceed your study timelines.
reduction in observation error rates
Our CNS suite of services apply the clinical expertise of WCG scientists and clinicians to mitigate the risks of bias, variability and human error, while addressing the root causes of failed and inconclusive CNS trials.
clinical experts ready to engage to review critical data across your study
We provide sponsors and CROs unmatched scientific competence and real-time access to assure every stage of your studies is achieving key clinical objectives – increasing your likelihood of success.
SITE ACTIVATION
DRUG SAFETY