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Public

AHA Response to FTC RFI on Employer Noncompete Agreements

the American Hospital Association thanks the Federal Trade Commission (FTC) for dismissing its appeals in Ryan, LLC v. FTC, No. 24-10951 (5th Cir.), and Properties of the Villages v. FTC, No. 24-13102 (11th Cir.), and acceding to the vacatur of the Non-Compete Clause Rule.
Employer Relations, Workforce, Physician Workforce, Legal/Regulatory ERM Domain
Public

AHA Response to FEMA RFI on Disaster Responses, Public Assistance Program

AHA's comment on our members’ experiences with the Federal Emergency Management Agency’s (FEMA) disaster responses, in particular the FEMA Public Assistance (PA) program
Disaster Preparedness
Public

AHA Comments on DEA Proposed Rule on Special Registrations for Telemedicine Prescribing

AHA comments regarding the Drug Enforcement Administration’s proposed rule for Special Registrations for Telemedicine and Limited State Telemedicine Registrations.
Telemedicine
Public

AHA Requests Flexibility Extension on DEA Telemedicine Prescribing

AHA comments to the Drug Enforcement Administration regarding their efforts to support the safe prescribing of controlled substances via telehealth. Indeed, during the COVID-19 public health emergency
Telemedicine

AHRMM LUC Comments to the FDA’s Draft Guidance for Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices

The AHRMM LUC members submitted comments and recommendations to the FDA's Draft Guidance for Select Updates for Unique Device Identification: Policy Regarding Global Unique Device Identification Database Requirements for Certain Devices. They recommend that information related to all Class I Medical Devices be included in the GUDID without exception.
Learning UDI Community, Unique Device Identifier (UDI), Supply chain management, Regulatory Compliance, Patient Safety Risk, Medical Device Safety

AHRMM LUC Comments to the FDA’s Communications About the Safety of Medical Devices

The AHRMM LUC members submitted public comments and recommendations at the FDA's November 2020 meeting related to the need to include the UDI in the recall process. They highlighted the prototype recall database and electronic submission form, as well as survey data supporting its creation.
Learning UDI Community, Unique Device Identifier (UDI), Medical Device Safety, Supply chain management, Regulatory Compliance, Patient Safety Risk, Medical Device Regulation

AHRMM Comment Letter to FDA RE: “Modernizing FDA’s Data Strategy”

In September 2019, FDA announced its Technology Modernization Actio
Learning UDI Community, Unique Device Identifier (UDI), Medical Device Safety, Supply chain management, Regulatory Compliance, Patient Safety Risk, Serious Adverse Events, Medical Device Regulation