From nonclinical modeling and artificial intelligence to clinical trial management and standardized data exchanges, we are committed to using data and technology to revolutionize how you bring products to market.
Clinical Data Management (CDM) is vital to properly perform clinical research. When executing data collection, W&P experts build data that is credible and comprehensive to drive an expedited process between drug development, approval, and market placement.
We understand that at the end of a trial, it’s all about the data. Starting with the creation of your custom clinical data management plan, through the database lock stage you’ll find W&P to be meticulous in every stage.
The same reliable clinical trial data management team with indication-specific expertise supports your project every step of the way. Our system features:
Tell us about your clinical trial data management needs Integrity matters, whether it’s describing your study data or the teams generating and managing your study data. Ensure integrity with W&P.
eClint® is a suite of data and technology enabling solutions designed to increase drug and medical device development efficiency, reduce timelines, improve compliance and drive commercialization for clinical trial development.
“With a real-time view across clinical trial processes, Clint CTMS improves operational efficiency, streamlines collaboration, and enables faster, higher-quality trial execution.”
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eClint® is a suite of data and technology enabling solutions designed to increase drug and medical device development efficiency, reduce timelines, improve compliance and drive commercialization for clinical trial development.
All-you-need eCRF for pre or post-market clinical studies.
Collect data directly from subjects via email and SMS.
Fully streamlined eCRF and ePRO for all types of clinical studies and RCTs.
GCP compliant ad hoc case-series data collection.
GCP compliant ad hoc case-series data collection.
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Increase the efficiency and
effectiveness of your clinical
trials with Xcellerate
Sample processing labs, clinical trial sites and offices in five continents provide the clinical reach and scale to manage complex global programs.
Tailored strategies consider the scientific, regulatory, and commercial factors that shape each trial, mitigating risk and advancing the development pathway.
Advanced trial-design approaches—including basket, umbrella, and adaptive trials—deliver biomarker driven clinical research. Deep experience in these highly complex trial designs maximizes both insights and efficiency.
Seasoned biostatisticians and statistical programmers deliver insight into every trial phase, from study design to regulatory submissions, all backed by meticulous documentation and data monitoring.
Sample inventories from a global network of labs supply real-time processing in 55 countries; consolidated data from central labs, screening labs, and specialty labs with clinical data create actionable reports.
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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