Analgesic Solutions
WCG is a global leader in accelerating clinical research by providing solutions that improve quality, efficiency, and human subject protections. With over 55 years of experience, WCG connects sponsors, CROs, sites, and participants through expertise, data, and technology to bring therapies to patients faster. The company is actively involved in cutting-edge research and education, including gene therapy and synthetic biology, and offers a wide range of services to support clinical trials and biosafety oversight.
Industries
Nr. of Employees
small (1-50)
Analgesic Solutions
5000 Centregreen Way, Suite 200, Cary, NC 27513
Patents
Products
IRB document management portal
A web-based IRB submission and document management portal that provides oversight, tracking and 24/7 access to IRB submissions and decisions.
Clinical Trial Management System (CTMS) platform
Platform to manage study lifecycle elements including enrollment, calendars, budgets, billing and links to electronic data capture.
Clinical trial listing and patient-matching service
Public-facing trial listing and patient discovery service to increase study visibility and match interested patients to appropriate trials.
IRB document management portal
A web-based IRB submission and document management portal that provides oversight, tracking and 24/7 access to IRB submissions and decisions.
Clinical Trial Management System (CTMS) platform
Platform to manage study lifecycle elements including enrollment, calendars, budgets, billing and links to electronic data capture.
Clinical trial listing and patient-matching service
Public-facing trial listing and patient discovery service to increase study visibility and match interested patients to appropriate trials.
Services
Centralized ethical review and approval services for study protocols and consent documents to ensure participant protection and regulatory compliance.
Management and administration of convened biosafety committee meetings and biosafety reviews for gene transfer and recombinant DNA research.
Focused in-person and workshop-based courses that cover synthetic biology, gene-editing technologies, cellular therapy mechanisms, protocol development, and mock IBC review exercises to build reviewer competency.
Consulting and technical review services to assist institutions and sponsors in establishing IBC oversight for gene transfer studies, developing biosafety plans, and conducting mock reviews or protocol walkthroughs.
Provision and management of independent medical, statistical and safety experts for blinded endpoint adjudication and ongoing safety monitoring in clinical trials.
End-to-end safety services including adverse event processing, aggregate reporting, medical information, and operational support for clinical and marketed products.
Centralized ethical review and approval services for study protocols and consent documents to ensure participant protection and regulatory compliance.
Management and administration of convened biosafety committee meetings and biosafety reviews for gene transfer and recombinant DNA research.
Focused in-person and workshop-based courses that cover synthetic biology, gene-editing technologies, cellular therapy mechanisms, protocol development, and mock IBC review exercises to build reviewer competency.
Consulting and technical review services to assist institutions and sponsors in establishing IBC oversight for gene transfer studies, developing biosafety plans, and conducting mock reviews or protocol walkthroughs.
Provision and management of independent medical, statistical and safety experts for blinded endpoint adjudication and ongoing safety monitoring in clinical trials.
End-to-end safety services including adverse event processing, aggregate reporting, medical information, and operational support for clinical and marketed products.
Expertise Areas
- Ethical review and human subject protection
- Clinical trial operations and start-up
- Participant recruitment, enrollment and retention
- Pharmacovigilance and drug safety
Key Technologies
- Clinical Trial Management Systems (CTMS)
- Electronic Trial Master File (eTMF) integration
- Electronic Clinical Outcome Assessment (eCOA/ePRO)
- Cloud-based IRB/document management portals
News & Updates
A virtual conference scheduled for October 20-24, 2025, available on demand until October 2026.
A virtual conference scheduled for October 20-24, 2025, available on demand until October 2026.