ORAQ is a Duke resource that our team relies on to navigate regulatory strategy
Read more here
Our services are outlined on our process page.
FastTrack currently works with projects that are classified as Class I and Class II medical devices. These devices are not considered to have high risk to the patient. If you do not know how to classify your device or idea, check out this resource from the FDA or reach out to ORAQ for a consultation.
Applicants must be a current Duke Faculty member, staff (e.g. Resident, Fellow, Researcher), or medical/graduate student. If you do not fit into these categories but are still interested in the program, feel free to contact us.