W&P offers end-to-end solutions for all your clinical research needs. W&P can be your ideal partner and guide throughout every step of your clinical trial, from scientific and regulatory support to compliance, pharmacovigilance, site engagement, and data management. Our expert staff, state-of-the-art facilities, and bespoke services enable you to enhance patient engagement, reduce risk, and gain higher quality data, all towards the ultimate goal of developing better treatments and improving patient outcomes.
With people across 70+ countries, our team provides comprehensive clinical trial services that streamline and
accelerate drug development at a global scale
W&P provides clinical research organization services throughout Europe. Efficiencies include faster patient recruitment due to the centralized healthcare systems in CEE countries and highly-engaged clinical trial investigators who produce high-quality work. We generally recommend our clients include a significant number of sites in CEE to ensure that their studies finish on schedule.
W&P’s APAC CRO services include a network of study sites which provide access to the diverse patient populations and disease states prevalent throughout Asia.
CRO in Seoul, South Korea
Our medical writers have strong scientific knowledge in most major therapeutic areas and develop clinical study design and protocols, document clinical study reports in compliance with guidelines such as MFDS, FDA, ICH-GCP/KGCP and EMA.We offer medical support, in close collaboration with our Clinical Operation, Biostatistics and Data management teams to ensure high-quality data and on-time reporting of study deliverables.
As part of W&P’s global clinical research services, we routinely conduct clinical trials throughout the Americas and are a leading CRO in the United States and Canada. We have existing relationships with over 20 sites throughout North America, giving you access to many of the world’s most prominent research institutions and investigators who are global leaders in their respective fields. These existing site relationships also streamline study start-up and operations, enabling efficient and high-quality clinical trials.
Our professionals apply their therapeutic, regulatory, and operational expertise to consistently solve the challenges taht arise during clinical projects.
Our seasoned biostatisticians and statistical programmers deliver insight into every phase of your trial, from study design to regulatory submissions, all backed by meticulous documentation and data monitoring.
We manage sample inventories across a global network of labs to supply real-time processing in 55 countries, then consolidate data from central labs, screening labs, and specialty labs with clinical data to create actionable reports.
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W&P offers end-to-end solutions for all your clinical research needs. W&P can be your ideal partner and guide throughout every step of your clinical trial, from scientific and regulatory support to compliance, pharmacovigilance, site engagement, and data management.
Our expert staff, state-of-the-art facilities, and bespoke services enable you to enhance patient engagement, reduce risk, and gain higher quality data, all towards the ultimate goal of developing better treatments and improving patient outcomes
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