The Avoca Group
The Avoca Group is a leading provider of quality and compliance solutions for the clinical research industry. With over 20 years of experience, they offer consulting, research, and collaborative services to help sponsors, CROs, and clinical service providers improve quality, ensure compliance, and increase efficiency in clinical trial execution. Their mission is to positively impact all clinical trials by supporting the industry in building industry-leading quality management, inspection readiness, and oversight systems.
Industries
Nr. of Employees
small (1-50)
The Avoca Group
Products
Knowledge Center repository (member toolkit)
A curated library of tools, templates, guidelines, metrics, and recordings to support clinical trial quality and oversight across the study lifecycle.
Annual Quality Consortium Summit and member events
Industry-wide summit, regional meetings, and recurring collaborative forums focused on quality, regulatory change, and operational best practices.
Knowledge Center repository (member toolkit)
A curated library of tools, templates, guidelines, metrics, and recordings to support clinical trial quality and oversight across the study lifecycle.
Annual Quality Consortium Summit and member events
Industry-wide summit, regional meetings, and recurring collaborative forums focused on quality, regulatory change, and operational best practices.
Services
Advisory and implementation services for clinical quality, inspection readiness, QMS design, and regulatory compliance across sponsors, CROs, and service providers.
Membership program providing access to a curated knowledge repository of tools, templates, metrics, and member-only collaborative events and recordings.
GCP training, metric workshops, interactive sessions, and tailored courses to upskill clinical research teams on quality, monitoring, and regulatory topics.
Design and implementation of study and program-level metrics, KRI/KPI definitions, dashboards, and benchmarking analyses.
Support for meeting EU Clinical Trial Regulation requirements, CTIS reporting workflows, serious breach reporting, and ICH E6 implementation planning.
Advisory and implementation services for clinical quality, inspection readiness, QMS design, and regulatory compliance across sponsors, CROs, and service providers.
Membership program providing access to a curated knowledge repository of tools, templates, metrics, and member-only collaborative events and recordings.
GCP training, metric workshops, interactive sessions, and tailored courses to upskill clinical research teams on quality, monitoring, and regulatory topics.
Design and implementation of study and program-level metrics, KRI/KPI definitions, dashboards, and benchmarking analyses.
Support for meeting EU Clinical Trial Regulation requirements, CTIS reporting workflows, serious breach reporting, and ICH E6 implementation planning.
Expertise Areas
- Clinical trial management
- Quality management systems (QMS)
- Risk-based quality management (RBQM)
- Inspection readiness and regulatory audit preparation
Key Technologies
- Centralized monitoring
- Risk-based monitoring frameworks
- Quality metrics and KRI/KPI toolkits
- eTMF / electronic TMF processes
News & Updates
A report on the implementation of ICH E6 (R3) guidance, available now.
A webinar demo of the Avoca Knowledge Center.
Details on how to implement ICH E6(R3) guidance with AQC support.
Discussion on how metrics can improve clinical trial quality and efficiency.
Recognized as part of the Inc. 5000 list of fastest-growing private companies in 2021.
Received the 2019 NJ Digi-tech Innovator Award.
A report on the implementation of ICH E6 (R3) guidance, available now.
A webinar demo of the Avoca Knowledge Center.
Details on how to implement ICH E6(R3) guidance with AQC support.
Discussion on how metrics can improve clinical trial quality and efficiency.
Recognized as part of the Inc. 5000 list of fastest-growing private companies in 2021.
Received the 2019 NJ Digi-tech Innovator Award.