HST.535 | Fall 2004 | Graduate

Principles and Practice of Tissue Engineering

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

Course Info

As Taught In
Fall 2004
Level