With decades of continuous, real-world data management and analysis experience, ActiGraph helps you generate evidence to gain regulatory approval and get life-saving drugs to patients, faster.

ActiGraph is ISO-13485:2016 certified, and our wearable technology is FDA 510(k) cleared Class II medical devices in the U.S. and adhere to regulatory standards worldwide.

ActiGraph leverages cloud, wireless and mobile technologies to provide flexible data capture and transfer configurations to support various study designs and methodologies, and integrations with other connected health sensors, ePRO tools, custom mobile applications, and third-party EDC platforms.

Our technology delivers near real-time data designed around the complexities of clinical research. With algorithms that are public and not proprietary, raw sensor data can be reprocessed indefinitely as new algorithms and analytic methods are developed by the scientific community.

From protocol development, endpoint selection and validation, algorithm refinement, onsite training, in-trial data screening and ongoing logistics to regulatory data submission and post hoc data analysis, ActiGraph provides the solutions and support to ensure efficient technology deployments, and the collection of clinically meaningful participant data.