Scientific & Regulatory
On-demand access to the industry’s largest network of medical, clinical, and statistical experts for your study.
On-demand access to the industry’s largest network of medical, clinical, and statistical experts for your study.
By combining expert scientific committee and safety data review experience across hundreds of clinical trials with a global knowledge base of 95% of all industry-sponsored protocols, WCG Scientific & Regulatory services provide sponsors and CROs unmatched scientific competence and real-time access to assure every stage of your studies is achieving key clinical objectives.
Only WCG provides sponsors and CROs such a comprehensive combination of expert review services—including Trial Design Review, Protocol Design Review, Data Monitoring Committees, Endpoint Adjudication, Drug Safety and Pharmacovigilance—under one roof.
When you choose WCG, you gain not only a broad range of scientific review and pharmacovigilance services, but also our astute judgment as to best compliance practices and state-of-the-art technology applied to your safety processes.
SafetyPortal provides global safety document distribution with real-time delivery, automated viewer tracking and robust reporting capabilities.
SafetyPortal not only streamlines safety report distribution, but also ensures that only those who need to see any given document receive it, reducing wasted time and expense.
You can rely on WCG because our team has been involved for decades in the pre- and post-approval process and are experts at avoiding the inherent hazards involved in bringing pharmaceutical products to market. Most importantly, we’ve gained incomparable knowledge about how proactively to mitigate these risks and protect your investment.
To explore how we can help with any or all of your product safety requirements, we suggest an exploratory conversation to assess your plans and how our capabilities can be leveraged to assist. To start, please simply fill out the form.