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Reimbursement for IVD Tests

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SKU: KLI5141105 Categories: Diagnostics Market Research, Oncology & Hematology Market Reports Pages: 60
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Description

What is the procedure, for establishing reimbursement for an IVD test product?  What companies have been successful and how?  What changes will IVD makers face in the near-term.  This Kalorama Information report, Reimbursement for In Vitro Diagnostic Tests, answers these questions and provides authoritative data for IVD business planners.

One of the critical factors for the success of an IVD product is reimbursement. Reimbursement is a critical component of the health care landscape and will continue to have a major impact on the continued usage of established products as well as product innovation and the market success of new technologies since products without solid reimbursement will not achieve widespread utilization and/or will not provide the revenues for their developers to continue to introduce new products.

This report, Reimbursement for In Vitro Diagnostic (IVD) Tests examines the U.S. reimbursement system for IVD tests, focusing on key issues of current concern to industry. It covers only commercialized tests, specifically excluding those that are developmental or used primarily for research purposes.

As part of its analysis, the report has the following:

  • Explanation of the Process for Reimbursement of IVD Products Under Medicare
  • Upcoming Medicare Reimbursement Cuts
  • Recent FDA Approvals of IVD Devices
  • Oversight of LDTs, Pilot IVD Triage Program, UDI Rule and Other Regulatory Initiatives
  • Office of the General Inspector Recommendations
  • ICD Codes, Laboratory NCD Codes and CLFS Test Codes
  • Gap-Fill Rates for Molecular Diagnostics
  • The Assessment of Novel Tests
  • Case Studies of Successful IVD Products and Lessons for New Entrants

The key open issues facing IVD reimbursement may be broadly grouped into four categories that comprise budget tightening, including Medicare cost cutting; outdated CLFS; FDA initiatives encompassing both rulemaking and new regulatory pathways; and challenges assessing new tests.

Historical information for this report was gathered from a wide variety of published sources including company reports and filings, government documents, legal filings, trade journals, newspapers and business press, analysts’ reports and other sources. Interviews with company representatives and other experts were conducted to capture the perspectives from industry participants’ point of view and assess trends. Case studies of successful reimbursement strategies are included to illustrate how product developers obtain reimbursement for new IVD tests.

Table of Contents

CHAPTER ONE: EXECUTIVE SUMMARY

Medical Device and In Vitro Diagnostics (IVD) Testing Reimbursement

Scope and Methodology

Introduction

Important Issues in IVD Reimbursement

Case Studies in Obtaining IVD Reimbursement

CHAPTER TWO: CMS AND PRIVATE INSURANCE REIMBURSEMENT FOR

IVDS

Overview

The U.S. Health Care Reimbursement System

History of IVD Reimbursement Under Medicare

Code Stacking

Billing for Stored Specimens

The Patient Protection and Affordable Care Act (PPACA)

FDA Oversight of IVDMIAs

ICD Codes

Laboratory National Coverage Determinations

New Tests

Molecular Diagnostics

Multi-Analyte Assays with Algorithmic Analyses

Recent IVD Device Approvals

CHAPTER THREE: IMPORTANT ISSUES IN IVD REIMBURSEMENT

Overview

Budget Tightening

Medicare Reimbursement Cuts

OIG Assessment

Outdated CLFS

FDA Initiatives

Oversight of LDTs

Pilot IVD Triage Program

UDI Rule

Challenges Assessing New Tests

Pharmacogenomic Tests

PSA Tests

CHAPTER FOUR: CASE STUDIES IN OBTAINING

IVD REIMBURSEMENT

Overview

AlloMap

MammaPrint

OncotypeDX

List of Exhibits

LIST OF EXHIBIT S

CHAPTER ONE: EXECUTIVE SUMMARY

Figure 1-1 FDA Approvals of IVD Devices

CHAPTER TWO: CMS AND PRIVATE INSURANCE REIMBURSEMENT FOR IVDS

Table 2-1 2013 CLFS Selected Test Codes

Table 2-2 List of ICD Codes, 2013

Table 2-3 Laboratory NCDs, 2013

Table 2-4 New and Reconsidered CLFS Test Codes, 2013 (Excludes Molecular Pathology & Multi-Analyte Assays with Algorithmic Analyses)

Table 2-5 2013 CLFS Gap-Fill Rates for Molecular Diagnostics

Table 2-6 Recent IVD Device Approvals

 

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