Full-Service CRO for Early Phase Clinical Development.
Agile and Collaborative CRO Services
Our CRO services can guide your journey through the clinic. Gain the comfort of a global, specialized team that uses an innovative, agile and collaborative approach to optimize all areas of your clinical development program. Our late phase development services are catered to organizations developing treatment in a wide variety of therapeutic areas, medical devices, and biologic and diagnostic. WCCT is dedicated to working together with our pharmaceutical and biotech industry sponsors to ensure that their development objectives are realized.
Why You Should Choose WCCT CRO Services:
Simplicity – we make navigating clinical trials easy
Quality – our services deliver meaningful results that exceed industry standards
Reliability – for over a decade, WCCT has been providing support services with a high repeat business rate
Flexibility – all of our development services are offered as a full suite or on an a-la-carte basis, such that we tailor our approach to your unique needs</
All of WCCT Global’s Project Managers are well-versed in managing Phase I-IV, full-service clinical projects. Our late phase project managers have 15+ years of experience.
WCCT will develop a comprehensive site project plan to optimize efficiency and resource allocation, ensuring that all sites have complete coverage and support.
During Study Start-Up, we will ensure that regulatory documents are accurate, complete, and in accordance with the sponsor requirements.
Clinical monitoring performed by highly-trained professionals with over ten years experience. We ensure all monitors have the educational background and experience necessary to successfully respond to your project’s unique needs.
From conception of a program or study, we can provide consulting on study design and analytical strategy which keeps in mind the most precise way to address study objectives within the current regulatory landscape.
WCCT Global offers full-service clinical regulatory affairs support from pre-IND meeting preparation through NDA submission, and all FDA correspondence which occurs in-between. Our team has a combined 45 years experience in the industry.