23 computer-graphics positions at Center for Devices and Radiological Health (CDRH)

FDA Development of a Queryable Technological Parameter Library for Energy-Based Surgical Devices Indexed by Indications for Use (IFU)

Center for Devices and Radiological Health (CDRH) | United States | about 1 hour ago

technical data into a centralized, queryable library or workspace. Build familiarity with the use of AI-enabled and regulatory informatics platforms, including ELSA, Python Vibe Coding, and the CDRH-CARS

FDA Postdoctoral Fellowship - Identification Criteria Development for Extractables and Leachables Non-Targeted Analysis

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 1 hour ago

Residents (LPR), and foreign nationals. Non-U.S. citizen applicants should refer to the Guidelines for Non-U.S. Citizens Details page  of the program website for information about the valid immigration

FDA Development of a General Surgery Devices Database and Analysis to Identify Key Technological Attributes and Trends

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 1 hour ago

-U.S. Citizens Details page of the program website for information about the valid immigration statuses that are acceptable for program participation. This program, administered by ORAU through its

FDA Digital Pathology Image Analysis Fellowship

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 1 hour ago

focused on the development of methods and tools in support of our regulatory science efforts in evaluating computational pathology (CPATH) devices. As a fellow, you will have the opportunity to learn about

FDA Interventional Radiological Imaging and Visualization (IRIS) Fellowship

Center for Devices and Radiological Health (CDRH) | Southern Md Facility, Maryland | United States | about 1 hour ago

efficient regulatory pathways, and assuring consumer confidence in devices marketed in the U.S. Research Project: The IRIS program addresses critical regulatory science challenges in three related and

FDA Artificial Intelligence and Machine Learning Fellowship

Center for Devices and Radiological Health (CDRH) | Southern Md Facility, Maryland | United States | about 1 hour ago

: The Artificial Intelligence Regulatory Science Program conducts regulatory science research ensuring safe and effective AI/ML-enabled medical devices across rapidly expanding healthcare applications including

FDA Fellowship - Development of Medical Device Extractable Database and Toxicological Risk Assessment Approaches

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 1 hour ago

Administration (FDA), located at Silver Spring, Maryland. Research Project: Two project opportunities are available in the Biocompatibility/Toxicology program in the FDA Center for Devices and Radiological Health

FDA Methodological Evaluation of Validation Approaches for AI/ML-Based Predictive Medical Devices for Regulatory Settings

Center for Devices and Radiological Health (CDRH) | United States | about 1 hour ago

available to U.S. citizens, Lawful Permanent Residents (LPR), and foreign nationals. Non-U.S. citizen applicants should refer to the Guidelines for Non-U.S. Citizens Details page of the program website

FDA Research Opportunity - Assessment of Bayesian Statistical Methods Applied in Regulatory Contexts

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 1 hour ago

the Guidelines for Non-U.S. Citizens Details page of the program website for information about the valid immigration statuses that are acceptable for program participation. This program, administered by ORAU

FDA Research Opportunity - Pediatric and Perinatal Devices

Center for Devices and Radiological Health (CDRH) | Silver Spring, Maryland | United States | about 1 hour ago

: The Pediatric and Perinatal Devices Program within the FDA’s Center for Devices and Radiological Health (CDRH) conducts regulatory science research aimed at advancing the development and evaluation of medical