US Regulatory Resources
Agency for Healthcare Research and Quality: Reducing Healthcare Carbon Emissions: A Primer on Measures and Actions for Healthcare Organizations to Mitigate Climate Change
The climate crisis is the single greatest public health challenge [...]
Federal Acquisition Regulation: Minimizing the Risk of Climate Change in Federal Acquisitions: Suggestions from the Association of Medical Device Reprocessors
The Association of Medical Device Reprocessors (AMDR) is the global [...]
The Reprocessing Solution: Reducing Greenhouse Gas Emissions and Lowering Healthcare Costs
The health sector accounts for almost 5% of all carbon [...]
Agency for Healthcare Research and Quality (AHRQ’s) Role in Climate Change and Environmental Justice: Suggestions from the Association of Medical Device Reprocessors
The Association of Medical Device Reprocessors (AMDR) is the global [...]
Comments to Council on Environmental Quality; Federal Agency Climate Adaption and Resilience Plans
We are pleased to have the opportunity to comment on [...]
Center for Disease Control and Prevention (CDC):
Reuse of Single-Use Medical Devices, Guideline for Disinfection and Sterilization [...]
2008 Government Accountability Office (GAO) Report:
Reprocessing Single-Use Devices, FDA Oversight Has Increased, and Available Information [...]
US FDA 2006 Testimony to Committee on Government Reform
US FDA 2006 Testimony to Committee on Government Reform
US FDA SUD Reprocessing Guidance, 2002 “Supplemental Validation Data”
Medical Device User Fee and Modernization Act of 2002, Validation [...]
2000 Government Accountability Office (GAO) Report:
Single-Use Medical Devices, Little Available Evidence of Harm From Reuse, [...]