Accredited Clinical Research

The Site Staff Qualifications Assessment and Onboarding Plan, Site Staff Training Plan, and documentation of the various associated training that may occur are a critical underpinnings of our research effort.   The documentation is current and complete illustrating to internal and external stakeholders the organization’s commitment to quality and compliance. 

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In the changing global regulatory environment, having appropriate documentation and best practices in place is critical to maintaining compliance. WCG Avoca’s Quality Consortium (AQC) offers a wealth of knowledge and tested leading practice tools and templates that ensure we are inspection ready.

Through participation in the AQC, along with more than 220 member pharma, biotech, site, niche clinical service providers, and CRO organizations, we collaborate in a progressive, pre-competitive environment with the shared objective of elevating quality and bringing key stakeholders in the clinical trials process into greater alignment.

As full members, we stay current on the latest challenges in the industry and have access to over 500 leading practices, tools, templates, dashboards, and process documents to assist with quality, risk management, and inspection readiness in clinical trial execution.

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