Improving outcomes, quality, safety, efficacy, and compliance.
If you are interested in working with us or learning more about our expertise, contact us here.
AceInfo supports the development of solutions for monitoring and analyzing public health data to better inform solutions for effective response and proactive prevention efforts.
We design processes including issue identification, tracking, workflow, resolution, as well as implement the right technologies that enable customers to effectively respond to incidents and crises.
Our technology solutions, including informatics portals, help track, monitor, and drive intervention for existing and emerging diseases and health risks.
We leverage scientific data integration expertise to support the tracking and monitoring of diseases and health risks.
Research and Development (R&D)
We build solutions that help R&D teams work more effectively, share data to inform, and augment all phases of discovery.
We provide the technology support R&D teams need to carry out their work including designing virtual lab environments.
Our teams support the full lifecycle of development including adjuvant discovery, product development, facilities management, clinical trials support, and regulatory submissions support.
Clinical Data Analytics
We develop tools and systems that help customers better integrate, analyze, manage, and interpret data.
Regulatory Information Management (RIM)
We design solutions that track and manage data across all phases of the medical product lifecycle.
Clinical Trial Data Management
Our team ensures data is supported at every step of the clinical trial from abstraction to regulatory filing.
Post Market Surveillance
Using advanced analytics to look for patterns, our customers proactively identify and characterize post market events for regulatory action.
With a focus on developing proven, extensible common data models, our solutions provide a framework that enables a consistent, scalable, enterprise-wide approach to regulatory review.
Together, AceInfo and Dovel develop solutions for managing compliance with all medical product regulatory standards.
Biomedical Information Management
We support our customers’ efforts to develop innovative computational approaches to biomedical information management and analysis.
Our team develops solutions that collect and analyze complex biological data for better understanding of processes affecting human health and disease.
Clinical Trials Data Management
Following regulatory compliant data processes and applying our team's health and science backgrounds, we help trials move smoothly and efficiently.
Clinical Data Analytics
With subject matter expertise in genomics and genetics informatics applications and IT expertise, our team helps customers better see and interpret collected data.
Tool Development and Implementation
We create interfaces that allow meaningful access to information to enable discovery and analysis.