Improving outcomes, quality, safety, efficacy, and compliance.

Today’s health organizations are serving diverse user populations, managing and securing vast amounts of complex data, and adhering to strict regulations, all while trying to innovate for more efficiency, sharing, and improved knowledge. Dovel helps organizations modernize their approaches and processes to better meet their critical mission needs.

If you are interested in working with us or learning more about our expertise, contact us here.

Public Health

Dovel develops solutions for monitoring and analyzing public health data to better inform solutions for effective response and proactive prevention efforts.

Incident/Crisis Management

Dovel designs processes including, issue identification, tracking, workflow, and resolution, as well as implements 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.

Disease Surveillance

Dovel leverages scientific data integration expertise to support the tracking and monitoring of diseases and health risks.

Research and Development (R&D)

Dovel builds solutions that help R&D teams work more effectively, share data to inform, and augment all phases of discovery.

R&D Support

We provide the technology support R&D teams need to carry out their work including designing virtual lab environments.

Vaccine Research

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

Dovel develops tools and systems that help customers better integrate, analyze, manage, and interpret data.

Regulatory Information Management (RIM)

Dovel designs 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

Dovel is using advanced analytics to look for patterns to proactively identify and characterize post market events for regulatory action.

Regulatory Submissions

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.


Dovel develops solutions for managing compliance with all medical product regulatory standards.

Biomedical Information Management

Dovel supports 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 our IT expertise, we help customers better see and interpret collected data.

Tool Development and Implementation

Dovel creates interfaces that allow meaningful access to information to enable discovery and analysis.

Deployed FDA’s first enterprise-wide LIMS system
Developed and deployed a cloud-based data solution for only hemovigilance Patient Safety Organization (PSO) in the country
Transformed technology approach for FDA's management of regulatory submissions