![]() Fully integrated clinical research solutionsAs a full service academic research organization, the AHRC is designed to take research questions from conception through execution, and then beyond, into knowledge translation. Our core services include methodology and biostatistical consulting; protocol and case report form development; project, data, site, and serious adverse event (SAE) management; financial and contract management; clinical monitoring; data analysis, and medical writing. The AHRC also has central lab and central diagnostic imaging capabilities through its partnerships across the University of Toronto.
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One of AHRC’s unique and core offerings is full support for researchers, including medical writing; biostatistics and methodology; data analysis; and reporting and protocol development.
Identifying, enabling and managing your research sites are critical to the success of your project. The AHRC has expertise in feasibility and site selection; site start-up processes; site communications through newsletters, meetings, webinars, and others; innovative recruitment strategies; SAE management; and other critical aspects of managing your study sites.
Innovation requires rigorous attention to the details of your project. Case report form development; regulatory support; budget development; financial management; and contractual management are all handled by the AHRC.
Our hospital and university affiliations allow the AHRC to offer access to industry-leading central lab capabilities and central medical imaging capabilities. You’ll have access to the cutting-edge equipment and clinicians you need for success.
RAVETM is a sophisticated data management system with user-configurable workflows, sophisticated eCRF design, complex edit checking, customizable security parameters, integrations of other data sources, and is 21 CFR Part 11 compliant. Data stored in RAVETM are housed locally.
The AHRC provides customized, quality clinical trial monitoring services to ensure your trial is carried out in accordance with the study protocol, ICH/GCP, FDA and Health Canada requirements, and sponsor requirements.