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FDA uses the following metrics to assess the impact of CERSI research projects. Any updates will be provided on this webpage.
Advancing Regulatory Science
Alignment with FDA regulatory science priority(s)
Enhancement of FDA resources/ expertise/ capacity
Facilitation of strategic relationships with expert groups and stakeholders (e.g., patients, industry, professional societies, healthcare providers)
Building FDA preparedness for rapid response to health emergencies and new developments in emerging regulatory science through strategic science alliances
Disseminating Scientific Knowledge
Scientific publications/ citations in literature
Presentations at conferences/ meetings/ FDA Advisory Committee meetings
Incorporation into training/ education curriculum
Media coverage
Data Sharing with public
Catalyzing Action
Adoption/ adaptation of findings by stakeholders/ use of findings in advocacy
Technology transfer to stakeholders
Subject of professional society meeting
Catalyst for future research
Improvements in consumer understanding
Adoption for use into medical practice
Informing Regulatory Decision-Making
Development or change in:
Reference materials/ standards
Surveillance strategies
Guidelines/ Guidance
Regulations
Compliance/ enforcement strategies
Inspection/ sampling strategies
External communication strategies
Labeling
Agency Policy
* Increasing impact on Public Health from left to right
