Medavante-ProPhase
WCG is a global leader in accelerating clinical research, providing solutions that improve the quality, efficiency, and safety of clinical trials. With over 55 years of experience, WCG connects sponsors, CROs, sites, and participants through expertise, data, and technology to bring therapies to patients faster while maintaining high standards of human subject protection. The company offers specialized solutions for CNS clinical trials and has a dedicated scientific leadership team in neurodegenerative and behavioral health disorders.
Industries
Nr. of Employees
medium (51-250)
Medavante-ProPhase
Products
Electronic research oversight SaaS platform
Cloud‑based platform for research oversight committees that supports electronic submission, review workflow, minute tracking and audit trails for IRBs and institutional committees.
Endpoint adjudication management platform
Web‑based adjudication and committee workflow system designed to present pre‑packaged clinical event data to global medical experts and capture adjudication decisions and reports.
Site communications and training platform
Integrated platform for investigator and site staff training, safety letter distribution, site document exchange, and automated study close‑out workflows.
Clinical trial listing and market intelligence service
Publication and data services that list active clinical trials and provide market intelligence, site relationship benchmarking and industry reports.
Clinical rater training and assessment toolkit
A clinician‑focused toolkit and platform for delivering validated rater training, outcome measure libraries, and documentation to support consistent assessment in CNS and psychiatric trials.
Electronic research oversight SaaS platform
Cloud‑based platform for research oversight committees that supports electronic submission, review workflow, minute tracking and audit trails for IRBs and institutional committees.
Endpoint adjudication management platform
Web‑based adjudication and committee workflow system designed to present pre‑packaged clinical event data to global medical experts and capture adjudication decisions and reports.
Site communications and training platform
Integrated platform for investigator and site staff training, safety letter distribution, site document exchange, and automated study close‑out workflows.
Clinical trial listing and market intelligence service
Publication and data services that list active clinical trials and provide market intelligence, site relationship benchmarking and industry reports.
Clinical rater training and assessment toolkit
A clinician‑focused toolkit and platform for delivering validated rater training, outcome measure libraries, and documentation to support consistent assessment in CNS and psychiatric trials.
Services
Full IRB review (full‑board, expedited, and continuing review), protocol amendment review, single‑IRB services for multicenter studies, and prioritized review pathways for urgent public‑health protocols.
Organization and management of endpoint adjudication committees and safety/DMCs, including expert identification, case packaging and secure review workflows.
Statistical design and analysis for clinical trials, interim analysis and DMC reporting, and statistical materials for regulatory interactions.
Recruitment campaigns, partnerships with patient communities and patient‑centric engagement to identify and enroll participants, including outreach for rare and genetic diseases.
Design and implementation of quality systems, inspection readiness, and oversight frameworks to incorporate quality‑by‑design in clinical operations.
Provision of benchmarking datasets, cost‑of‑trial studies and performance reports to identify operational cost drivers and support budgeting and process improvements.
Full IRB review (full‑board, expedited, and continuing review), protocol amendment review, single‑IRB services for multicenter studies, and prioritized review pathways for urgent public‑health protocols.
Organization and management of endpoint adjudication committees and safety/DMCs, including expert identification, case packaging and secure review workflows.
Statistical design and analysis for clinical trials, interim analysis and DMC reporting, and statistical materials for regulatory interactions.
Recruitment campaigns, partnerships with patient communities and patient‑centric engagement to identify and enroll participants, including outreach for rare and genetic diseases.
Design and implementation of quality systems, inspection readiness, and oversight frameworks to incorporate quality‑by‑design in clinical operations.
Provision of benchmarking datasets, cost‑of‑trial studies and performance reports to identify operational cost drivers and support budgeting and process improvements.
Expertise Areas
- Ethical review and IRB oversight
- Clinical trial design and study planning
- Endpoint adjudication and committee management
- Biostatistics and statistical consulting
Key Technologies
- Electronic IRB and research oversight (SaaS) systems
- Adjudication workflow platforms
- Clinical Trial Management Systems (CTMS)
- eCOA / ePRO platforms
News & Updates
A virtual event on October 20-24, 2025, with on-demand access until October 2026.
Donald Deieso and Dawn Flitcraft honored for their efforts to advance patient-centric clinical trials.
A virtual event on October 20-24, 2025, with on-demand access until October 2026.
Donald Deieso and Dawn Flitcraft honored for their efforts to advance patient-centric clinical trials.