Midlands Independent Review Board (MLIRB)
WCG is a global leader in accelerating clinical research, serving biopharmaceutical and medical device companies, CROs, research institutions, and site partners. With over 55 years of experience, WCG offers expertise, next-generation data, insights, and tech-enabled solutions to improve study efficiency, safety, and outcomes while ensuring human participant protection. WCG's mission is to connect stakeholders and bring life-saving therapies to patients faster.
Industries
Nr. of Employees
small (1-50)
Midlands Independent Review Board (MLIRB)
Products
Study acceleration platform
A technology-enabled platform that combines feasibility, site-matching, and enrollment analytics to reduce study timelines and streamline study planning and execution.
Electronic clinical outcome assessment platform
Platform for electronic capture of clinician- and patient-reported outcomes and eSource integration to support data quality and regulatory submissions.
Feasibility and site-matching analytics platform
Analytics tools and databases leveraging historical site performance to assess feasibility and identify optimal investigative sites.
Enrollment management and patient-matching service
Services and digital listings to connect potential participants with trials and manage enrollment progress.
Cloud-based clinical collaboration and CTMS platforms
Hosted clinical trial management and collaboration platforms for study build, site communication, and document management.
Clinical trial listing service
Public-facing clinical trial listing and patient-facing matching service to facilitate participant identification and recruitment.
Study acceleration platform
A technology-enabled platform that combines feasibility, site-matching, and enrollment analytics to reduce study timelines and streamline study planning and execution.
Electronic clinical outcome assessment platform
Platform for electronic capture of clinician- and patient-reported outcomes and eSource integration to support data quality and regulatory submissions.
Feasibility and site-matching analytics platform
Analytics tools and databases leveraging historical site performance to assess feasibility and identify optimal investigative sites.
Enrollment management and patient-matching service
Services and digital listings to connect potential participants with trials and manage enrollment progress.
Cloud-based clinical collaboration and CTMS platforms
Hosted clinical trial management and collaboration platforms for study build, site communication, and document management.
Clinical trial listing service
Public-facing clinical trial listing and patient-facing matching service to facilitate participant identification and recruitment.
Services
Independent ethical review, centralized IRB-of-record services, and IRB coordination for multi-site studies.
Administration of institutional biosafety committees, biosafety review for gene transfer research, and Pre-RAC review support.
Design and operational management of endpoint adjudication committees and independent safety monitoring committees.
Multichannel recruitment, on-site enrollment assistants, community outreach, and partnerships with patient communities to identify and engage trial participants.
Regulatory-compliant safety operations including case processing, reporting, and safety program management for clinical and marketed products.
Consulting and operational services to incorporate genetic information into trial design, recruitment, and patient management, including genetic counseling and test interpretation.
Independent ethical review, centralized IRB-of-record services, and IRB coordination for multi-site studies.
Administration of institutional biosafety committees, biosafety review for gene transfer research, and Pre-RAC review support.
Design and operational management of endpoint adjudication committees and independent safety monitoring committees.
Multichannel recruitment, on-site enrollment assistants, community outreach, and partnerships with patient communities to identify and engage trial participants.
Regulatory-compliant safety operations including case processing, reporting, and safety program management for clinical and marketed products.
Consulting and operational services to incorporate genetic information into trial design, recruitment, and patient management, including genetic counseling and test interpretation.
Expertise Areas
- Clinical trial management
- Regulatory compliance and IRB/IBC oversight
- Patient recruitment and retention
- Precision medicine and genetics integration
Key Technologies
- Electronic clinical outcome assessment (eCOA/ePRO)
- eSource data capture
- Electronic trial master file (eTMF) integration
- Clinical trial management systems (CTMS)
News & Updates
Breaking Barriers: Mastering the Challenges of GLP-1 Drug Trials
Webinar on challenges and solutions in GLP-1 drug trials.
DIA 2025
WCG's participation in the DIA 2025 conference.
AACI CRI 2025
WCG's involvement in the AACI CRI 2025 event.
WCG Clinical Services Division Opens Office in Japan
Expansion of WCG's presence in Asia to support global clinical trials.
WCG Acquires KMR Group and MCC
WCG expands its market insights and intelligence services through acquisitions.
WCG Partners with InformedDNA
Strategic partnership to support genetics and precision medicine in trials.
Breaking Barriers: Mastering the Challenges of GLP-1 Drug Trials
Webinar on challenges and solutions in GLP-1 drug trials.
DIA 2025
WCG's participation in the DIA 2025 conference.
AACI CRI 2025
WCG's involvement in the AACI CRI 2025 event.
WCG Clinical Services Division Opens Office in Japan
Expansion of WCG's presence in Asia to support global clinical trials.
WCG Acquires KMR Group and MCC
WCG expands its market insights and intelligence services through acquisitions.
WCG Partners with InformedDNA
Strategic partnership to support genetics and precision medicine in trials.