Safety of Atrial Fibrillation Ablation Registry Initiative (SAFARI): Where we are today

Similar documents
Faster, More Efficient Innovation through Better Evidence on Real-World Safety and Effectiveness

Real-World Evidence: A CDRH Perspective

Registry of Patient Registries (RoPR) Policies and Procedures

Rare Disease Registries

FDA Vision for Innovative Surveillance of Orthopedic Implants

Professional Biography

Collaborative Communities: It Really Does Take a Village

PLAN OF ACTION FOR IMPLEMENTATION OF 510(K) AND SCIENCE RECOMMENDATIONS

Confronting the Challenges of Rare Disease:

SIMPLE SOLUTIONS. BIG IMPACT.

Best Practices for emeasure Implementation. Breakout Session #2: Implementation in Office-Based Practice Settings

Topic: CAP s Legislative Proposal for Laboratory-Developed Tests (LDT) Date: September 14, 2015

MULTIPLE SCLEROSIS SCIENTIFIC RESEARCH FOUNDATION (MSSRF) MULTI-CENTRE, COLLABORATIVE TEAM GRANT (Team Grant) PROGRAM GUIDE

REQUEST FOR PROPOSALS MING HSIEH INSTITUTE FOR RESEARCH ON ENGINEERING-MEDICINE FOR CANCER 2015 RESEARCH AWARD

FDA s Office of Regulatory Affairs: Violation Trends & Medical Device Update

Institute of Medicine Standards for Systematic Reviews

Guidance for Developing Payment Models for COMPASS Collaborative Care Management for Depression and Diabetes and/or Cardiovascular Disease

BONE STRESS INJURIES

Population Health Management Tools and Strategies to Support Care Coordination An InfoMC White Paper April 2016

Making the most of patient registries

World Accreditation Day Webinar

METHODOLOGY. Transparency. Conflicts of Interest. Multidisciplinary Steering Committee Composition. Evidence Review

November 7, Division of Dockets Management (HFA-305) Food and Drug Administration 5630 Fishers Lane, Room 1061 Rockville, MD 20852

Clinical Development Process 2017

EP LAB BENCHMARKING WHITEPAPER

On April 19, 2007, the National Working Group on

Better Medical Device Data Yield Improved Care The benefits of a national evaluation system

DynaMed Presentation. PhD. of strategic management Medical Library MUMS. Sima Mohazzab Hosseinian

Latham & Watkins Corporate Department

Statement for the Record. American College of Physicians. Hearing before the House Energy & Commerce Subcommittee on Health

Medicare s Impact on Cardiology Drugs and Devices During Clinical Research

Lessons from the EMA Patient Registries Initiative

Duke-Margolis Center: Overview And High Priority Projects in Biomedical Innovation and Payment

REQUEST FOR PROPOSALS MING HSIEH INSTITUTE FOR RESEARCH ON ENGINEERING-MEDICINE FOR CANCER

Alpha-1 Foundation Letter of Intent and Full Application Instructions

ICH Regulators Forum. Dr Peter Arlett EU

Starting the Conversation A SWOT, So What, & Now What? Summary, Implications & Next Steps

Alpha-1 Foundation Letter of Intent Application Instructions

Strengthening Patient Care: Building an Effective National Medical Device Surveillance System. February 2015

DANNOAC-AF synopsis. [Version 7.9v: 5th of April 2017]

Artificial Intelligence Changes Evidence Based Medicine A Scalable Health White Paper

Apps at the Point Of Care

7/7/17. Value and Quality in Health Care. Kevin Shah, MD MBA. Overview of Quality. Define. Measure. Improve

HIT and Medicaid: Opportunities for States Part I of a three part series on the State Alliance for E-Health E

Collaboration of the Hybrid AF Patient: Role of Advanced Practice Providers. Jennifer Walker, RN, MSN, ANP-BC UNC Center for Heart and Vascular Care

APLAR- Center of Excellence Evaluation Form

Defining an Outcome Measures Framework for Global Surgery

European Patients Academy on Therapeutic Innovation

ERN Assessment Manual for Applicants

Understanding and improving the quality of medication use: Research in Clinical Pharmacy starting from Academia. Anne Spinewine

2017 Oncology Insights

Terms of Reference: ALS Canada Project Grant Program 2018

Measure Applications Partnership (MAP)

Organizations in Nuclear Medicine Part IV- Others of Importance. Bennett S. Greenspan, MD SNM MWM Orlando, FL January 27, 2012

ABMS Organizational QI Forum Links QI, Research and Policy Highlights of Keynote Speakers Presentations

Medicare Part C Medical Coverage Policy

Registries for Evaluating Patient Outcomes: A User s Guide Second Edition

- Proposal for a Regulation on HTA- Ioana Siska, MD, PhD DG SANTE - Health Systems and Products Medical Products: safety, quality, innovation

Health Technology Assessment (HTA) Good Practices & Principles FIFARMA, I. Government s cost containment measures: current status & issues

Patient Registry Initiative- Strategy and Mandate of the Cross-Committee Task Force

Introduction to Coverage Analysis Part 1. Amanda Miller, Training Program Manager Derek McCormick, Operations Manager October 14, 2016

Potential of the use of electronic patient information for clinical research in the pharmaceutical industry

2010 Operational Plan - Project Description. 1

Movember Clinician Scientist Award (CSA)

DRAFT OPINION. EN United in diversity EN. European Parliament 2018/0018(COD) of the Committee on Industry, Research and Energy

Health System Leadership and Improvement Research at KPSC: Care Improvement Research Team (CIRT)

HEALTH TECHNOLOGIES FUND ROUND 3 BRIEFING

Retrospective Chart Review Studies

Registries for Evaluating Patient Outcomes:

Consensus Recommendations on Rater Training and Certification

Cardiac Certification. Achieving excellence beyond accreditation

SCREENING SCOPING ASSESSMENT RECOMMENDATIONS REPORTING MONITORING & EVALUATION

Rt hon Jeremy Hunt MP Secretary of State for Health and Social Care. Letter by to Dear Jeremy

Office of Surveillance, Epidemiology, and Laboratory Services Epidemiology and Analysis Program Office

Application Instructions for PEDSnet Scholars Institutional K12 Award Last Updated:

Quality ID #348: HRS-3 Implantable Cardioverter-Defibrillator (ICD) Complications Rate National Quality Strategy Domain: Patient Safety

Pharmacy Schools Council. Strategic Plan November PhSC. Pharmacy Schools Council

1. Introduction, purpose of this Standard Operating Procedure (SOP)

1. Introduction, purpose of this Standard Operating Procedure (SOP)

European Patients Academy (EUPATI) Update

2018 Call for Projects on ALS Research

Why do we need an addendum to ICH E6?

July 7, Dear Mr. Patel:

Evaluation at the Innovation Center

QUALITY IN PULMONARY REHABILITATION

MDEpiNet RAPID Meeting

Introduction Patient-Centered Outcomes Research Institute (PCORI)

SBAR: NCDR Registries Initiation and Feedback Phase

Survey into the diagnosis, management and treatment of patients with Atrial Fibrillation

Pay-for-Performance: Approaches of Professional Societies

ESF Peer Review Services

Implementing and Improving: Behavioral Health Quality

UConn Health Office of Clinical & Translational Research Standard Operating Procedures

Patient-Clinician Communication:

Year in Review ro ils RO ILS

Pathology & Laboratory Medicine Lower Mainland Consolidation Project V3.10

Contains Nonbinding Recommendations. Draft Not for Implementation

MDUFA Performance Goals and Procedures Process Improvements Pre-Submissions Submission Acceptance Criteria Interactive Review

Focus on Medical Device: A conversation about Case for Quality. September 22, 2017

Community Engagement & Research

Transcription:

Safety of Atrial Fibrillation Ablation Registry Initiative (SAFARI): Where we are today Benjamin C. Eloff, Ph.D. Senior Scientific Program Manager Office of the Chief Scientist, FDA

The SAFARI Initiative AF ablation techniques and devices developed and refined rapidly Guidelines, consensus statement, AHRQ review published relying on current state of evidence, and noting limited follow-up data and limited generalizability of data. FDA recognizes similar gaps in data generated in premarket studies as discussed in September 2007 panel meeting FDA proposes a project through CSRC to develop a publicprivate partnership (PPP) to identify and fill known gaps in data April 2009, FDA hosts first workshop for SAFARI ACC, HRS, AdvaMed, CSRC, & FDA joined together to lay groundwork for the structure of the SAFARI partnership

Basic Steps in Developing PPPs with FDA (not comprehensive! not consecutive!) Start with the Public Health Need, SCIENCE! Identify Priorities for multiple stakeholders Identify gaps/avoid duplication e.g. biomarkers: Hold expert workshop, Identify partners etc. Leverage resources/expertise Identify partners: define roles/responsibilities Co-develop: proposals, budgets, timelines etc. Implement joint projects Share data in public domain as quickly as appropriate Some Benefits Industry: Postmarket trial data, Hypothesis generation FDA: Data for guidance development and regulatory mission ACC/HRS: Best Practices, Clinical Data CMS & Payers: Data for reimbursement policy decisions Patients: faster, safer and cheaper medical products!!!!

SAFARI Mission To facilitate a national pan-stakeholder collaboration supporting the design, implementation, and maintenance of a logistically feasible registry platform for systematic data collection characterizing the safety and effectiveness of on- and off-label real world atrial fibrillation ablation. The intention of this registry will be to inform the development of reliable knowledge, practice guidelines, and to better inform regulatory processes in relationship to the safety of medical products used in the diagnosis, ablation and subsequent treatment of atrial fibrillation.

SAFARI Objectives Establish a transparent, nationwide registry for collecting data related to AF ablation procedures Publicly report the data contained in the registry to inform the public health Specifically, the SAFARI partnership will: 1. Develop a framework for collaboration with participation from multiple stakeholders, resulting in an administrative infrastructure to facilitate joint activities in the study of ablation therapies for AF. 2. Support efforts to bridge the knowledge gaps that exist in the field of AF ablation. 3. Ensure that information resulting from these collaborative efforts is appropriately made available to stakeholders and the public. 4. Inform stakeholders, clinicians, and patients, through joint publications, regulatory guidance documents, workshops, and other educational and outreach efforts, of any potential safety risks associated with AF ablation. 5. Make recommendations on labeling of AF ablation devices, based on available data, and to inform regulatory decision-making. 6. Inform future activities, including clinical trials and the application of ablation therapy to treat AF.

Stakeholder Community Industry Payers Government Academia Professional Societies Hospitals Steering Executive Operations Budget Ad hoc Meeting Registry development team Registry implementation team Data quality team Data use & publications team

Today s Meeting and Next Steps Establish Steering and modify/implement governance Continue outreach to interested stakeholders Summarize, incorporate, and publish feedback from this meeting Secure funding for pilot registry

Thank You Meeting Planning Sana Al-Khatib Muriel Corcoran Ruey Dempsey John Finkle Daniel Frisch Isabelle LeBlanc Kristi Mitchell Kathy Pontzer Jeremy Ruskin Executive Operations Peter Kowey (Co-Chair) Ben Eloff (Co-Chair) Marcia Yaross Hugh Calkins Stephen Hammill Mitchell Krucoff Ellen Pinnow CSRC staff Valarie Morrow Valerie Bailey Eva Hill