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Clinical Best Practices
Heart Rhythm Society Health Policy Principles
The Heart Rhythm Society’s advocacy efforts focus on issues of critical importance to patients with heart rhythm disorders, including the commitment to evidence-based, guidelines-driven, affordable…
January 24, 2020

Educational Materials
Food & Drug Administration (FDA)
The Food and Drug Administration is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological…
January 24, 2020

Clinical Documents
2020 ACC / AHA / ASE / HRS / ISACHD / SCAI / SCCT / SCMR / SOPE Appropriate Use Criteria for Multimodality Imaging During the Follow-up Care of Patients with Congenital Heart Disease
This document addresses only the follow-up of patients with established congenital heart disease using various cardiovascular imaging modalities.
January 6, 2020

Comment Letter
HRS Submits Comments to Inform CMS 2021 Quality Programs
HRS submitted comments on the National Quality Forum’s Measure Applications Partnership (MAP) which provides guidance to the U.S. Department of Health and Human Services (HHS)…
December 2, 2019

Guidelines & Protocols
2020 Average Medicare Fees for EP Services
November 21, 2019 – The average Medicare physician fees for EP services…
November 21, 2019

Clinical Documents
"Real-World" Observational Studies in Arrhythmia Research: Data Sources, Methodology, and Interpretation
This document describes the usual data sources for observational studies, reviews common and important techniques, overviews the proper interpretation of results, and finally makes appropriate recommendations regarding…
November 14, 2019

Comment Letter
HRS Comments on FDA’s 2020 Guidance Priorities
The Food and Drug Administration’s (FDA) Center for Devices and Radiological Health (CDRH) has released its final and draft guidance publication priorities for the 2020…
November 13, 2019

2019 EHRA International Consensus Document on How to Prevent, Diagnose, and Treat Cardiac Implantable Electronic Device Infections
November 8, 2019—The aim of this document is to describe the current knowledge on…
November 8, 2019

Comment Letter
Industrial Ethylene Oxide Sterilization of Medical Devices
A Food and Drug Administration (FDA) committee is addressing industrial ethylene oxide (EtO) sterilization of medical devices and its role in maintaining public health.
October 22, 2019
Comment Letter
CV Community Voices Concerns About a Potential Mandate for Open Access to Publicly Funded Research
January 23, 2020