AHRM Inc. is a full service Contract Research Organization (CRO) with a focus in Health Economics and Outcomes Research (HEOR). By providing the ability to integrate both clinical and economic research into one protocol or study, AHRM Inc. can support FDA, Health Authority and Payor requirements typically in the same study protocol during the health technology development period for pharmaceuticals and medical devices.
For pharmaceuticals or devices already approved, Applied Healthcare Research Management Inc. can provide extensive guidance and support to develop, implement and manage trials in North America and Europe, or leverage existing data to develop and publish economic models targeted at payors or to support reimbursement.
Located at the New York State Center of Excellence in Bioinformatics & Life Sciences (COE) building since 2008, Applied Healthcare Resource Management Inc. has built a positive reputation with clients based on performance, professionalism and cost efficient execution of both Clinical Trial and Outcomes Research engagements. AHRM Inc. has conducted both clinical and outcomes research across most major therapeutic categories in North America, Europe and Latin America.
AHRM has extensive experience running and reporting RWE studies across the US and Europe using data abstracted from medical records or EMR data. AHRM is currently piloting a smart card technology linked to a patients EMR. Once fully deployed, AHRM will have access to de-identified EMR from around the world.
HEOR experience across every major therapeutic category.
Manuscripts, Posters, Publication Planning, Value Dossier, Clinical Summary Report (CSR), Presentations and White Papers.
Identification and recruitment of key individuals to generate informative data to support protocol development, health technology target population, health technology development, payor requirements, patient satisfaction and employer needs.
Collection, completion and submission of all required IRB materials for initial review, amendments and continuing reviews
Collection of and analysis of data using surveys or input from advisory boards.
Identification, screening and recruitment of sites based on study objectives.
Design and generation to provide standardized data collection to meet analysis requirements
EDC Development and Maintenance – Development of remote data capture systems which allows for real time monitoring of eCRF completion, data management and data analysis. These capabilities can expedite database lock timeframes
Comprehensive review and analysis of data quality. Query generation and resolution to ensure clean datasets used for reporting.
Clinical monitoring of your selected study sites as detailed in the clinical monitoring plan.
Analysis, sample size determination (clinical or economic), statistical analysis plan (SAP), interpretation, and inference of trial data.
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