The following four areas were designated for improvement. They are:
![](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/ti-bullet.gif) |
"Report of the Postmarket Transformation Leadership Team: Strengthening FDA’s Postmarket Program for Medical Devices" which provides an action plan for changes to the medical devices postmarket program. (November 2006) |
![Text](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker1.gif) |
![pdf](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker2.gif) |
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Questions & Answers - External Audience (November 2006) |
![Text](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker1.gif) |
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Press Release (November 2006) |
![Text](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker1.gif) |
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![](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/ti-bullet.gif) |
Ensuring the Safety of Marketed Medical Devices: CDRH’s Medical Device Postmarket Safety Program, which documents the postmarket inventory and discusses the CDRH postmarket program. (January 2006) |
![Text](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker1.gif) |
![pdf](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker2.gif) |
![](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/ti-bullet.gif) |
A separate Synopsis and Recommendations document provides a list of initial action steps the Center will take to strengthen postmarket effectiveness. (January 2006) |
![Text](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker1.gif) |
![pdf](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker2.gif) |
![](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/ti-bullet.gif) |
A presentation titled "Ensuring the Safety of Marketed Medical Devices" by Dr. Daniel Schultz, Director, Center for Devices and Radiological Health (January 4, 2006) |
![Text](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker1.gif) |
![PowerPoint](https://webarchive.library.unt.edu/eot2008/20090512003518im_/http://www.fda.gov/cdrh/images/linker3.gif) |