Collaboration Details

Print  Close

Title of Collaborative Activity:

Mobile Applications for Data Collection on Adverse Events of Medication or Device During Public Health Emergencies

Description of Collaborative Activity:

NLM and the U.S. Food and Drug Administration (FDA) established a partnership to explore the development, assessment, and utilization of mobile applications to disseminate and exchange scientific information and data concerning reported adverse events from the use of a medication or medical device approved under the Emergency Use Authorization in a public health emergency or disaster.

Type of Collaborative Activity:

Resource Development

Year the Collaborative Activity Originated:


NIH Participating Institutes/Centers/Office of the Director:


HHS Agency Collaborators on this Activity: