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67 Results Found

Issue Brief
Alarm Safety Management
This learning lab covers alarm safety management in the health care supply chain field.
Capital Equipment, Change Management, Products and Services Contracting, Regulations and Regulatory Advocacy, Leadership
Toolkits/Methodology
Guidance for Writing Comments
How to write a constructive, information-rich comment that clearly communicates and supports its claims to have an impact on regulatory decision making.
Disaster/Outbreak Preparedness, Legislation and Legislative Advocacy, Regulations and Regulatory Advocacy, Procurement
Letter/Comment
IRS Issues Final Rule Implementing Medical Device Excise Tax
An announcement of the Final Rule issued by the IRS.
Capital Equipment, Distribution, Regulations and Regulatory Advocacy, Procurement
Request for Proposals (RFP)
Bed Management System RFP
A sample of a bed management RFP covering all the basics. Download the document and tailor it to your needs.
Cost Management, Legislation and Legislative Advocacy, Regulations and Regulatory Advocacy, Medical Device Technology
Issue Brief
Medical Device Excise Tax - What You Should Know
The Medical Device Excise Tax, a component of the Affordable Care Act, is approaching implementation at the beginning of 2013. The tax is intended to provide an estimated $20 billion in tax revenues to help pay for the expansion of health coverage to 32 million uninsured Americans. Healthcare supply chain leaders have until May 7, 2012, to comment on the way in which the Internal Revenue Service (IRS) intends to implement this new tax.
Cost Management, Financial Management, Regulations and Regulatory Advocacy, Procurement
Advisory
Medical Device Tax Next Steps
The medical device excise tax is a feature of the Affordable Care Act. It is important to be knowledgeable about the tax and its effects.
Products and Services Contracting, Legislation and Legislative Advocacy, Physician Preference Items (PPI), Regulations and Regulatory Advocacy, Suppliers, Procurement
Letter/Comment
The Official Comment of AHRMM to the United States Department of Health and Human Services Food and Drug Administration (FDA) regarding Unique Device Identification for Medical Devices Docket No. FDA-2011-N-0090
AHRMM comments to the FDA regarding an amendment to the UDI proposed rule to address the UDI implementation time frame required by the 2012 Food and Drug Administration Safety and Innovation Act (FDASIA).
Cost, Quality and Outcomes (CQO) Movement, Data Standards, Materials Management Information System (MMIS), Regulations and Regulatory Advocacy, Suppliers, Leadership