Lecture Notes
s4i_fda.pdf
Description:
This resource includes information about federal agencies that regulate medical devices and tissue engineered products, US FDA organization, FDA approval process, FDA history, FDA device classification, what is premarket notification, substantial equivalence, premarket approval, PMA data requirements, federal regulatory issues, ISO, definition and examples of medical devices, marketing applications, internet access to FDA documents, tissue related documents and FDA approval process.
Resource Type:
Lecture Notes
pdf
928 kB
s4i_fda.pdf
Course Info
Instructors
Departments
As Taught In
Fall
2004
Level
Learning Resource Types
notes
Lecture Notes