Guidance for Writing Comments

By AHRMM
How to write a constructive, information-rich comment that clearly communicates and supports its claims to have an impact on regulatory decision making.
 

Related Resources

White Papers
The Critical Link Between Cost, Quality, and Outcomes (CQO) and Unique Device Identification (UDI) White Paper
In an effort to capture broader insights on UDI adoption from across the health care field, AHRMM, with participation by the FDA, held LUC Dat
e-Learning
CMRP Procurement and Product Value Analysis Course
e-Learning
CMRP Strategic Planning, Leadership, and Compliance Course
Webcast
UDI: Value Beyond Compliance
In this AHRMM webcast, Karen Conway, executive director of industry relations and value at GHX discusses her research with the FDA on the val
Webcast
UDI and MU3: What Data Goes in the Item Master?
Susan Morris, CMRP, FAHRMM, health care executive, Cerner Corporation, explains the different parts of the Unique Device Identifier (UDI) and
Guides/Reports
Low Unit of Measure (LUM) UDI Single Device Work Group Report
Download Report