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.

Choose a clinical data management team with W&P

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.

End-to-end coverage for your clinical data management needs

The same reliable clinical trial data management team with indication-specific expertise supports your project every step of the way. Our system features:

Clinical database management start-up

  • Develop custom clinical trial data management plan based on your protocol, study site needs, and your needs
  • Use best EDC for your needs
  • Design CRFs and write CRF guidelines
  • Coordinate data-in

Clinical database development

  • Build and screen the database, including testing and QC
  • Coordinate user acceptance training (UAT) with sponsor and study site

User administration

  • Set up accounts
  • Conduct training

Clinical database conduct

  • Data Cleaning
  • Query Resolution
  • Medical Coding
  • External Vendor Data Transfers & Reconciliation
  • SAE Reconciliation
  • Ongoing EDC Metrics, Clean Submit Report
  • ‘SMART’ Patient Profiles

Clinical database lock

  • Obtain PI signature
  • Lock CRFs
  • Generate final datasets
  • Site CRF Archival CDs
  • Decommission EDC

Tell us about your clinical trial data management needs

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®:Manage Trials End-to-end with a Modern CTMS

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.”

Trial study design

  • Protocol trial design tool
  • Patient intelligence

Patient & site recruitment

  • Trial recruitment analysis and forecasting
  • Site list tool
  • Spatial cluster analysis

Study risk evaluation

  • Risk assessment & categorization
  • Risk & issue management
  • Risk review

Operational insights

  • Action alerts
  • CRA dashboard
  • Study dashboard
  • Portfolio dashboard

Data quality & access

  • Medical review
  • Staistical review
  • Data review
  • Clinical trial data warehouse
  • Operational data warehouse

Central lab trial testing

  • Lab sponsor portal
  • LabLink+
  • Lab investigator portal

Product access

  • Patient access toolkit
  • Intelligence dashboard

Patient safety

  • Case management
  • Safety reporting


Results Available Wherever You Are

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.




Increase the efficiency and
effectiveness of your clinical
trials with Xcellerate

W&P Clinical Trial Services

Global Clinical Trial Footprint

Sample processing labs, clinical trial sites and offices in five continents provide the clinical reach and scale to manage complex global programs.

Clinical Development Strategy

Tailored strategies consider the scientific, regulatory, and commercial factors that shape each trial, mitigating risk and advancing the development pathway.

Clinical Development Strategy

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.

Clinical Sample Management

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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