The World Market for In Vitro Diagnostics, 2005
The world market in 2005 for In Vitro Diagnostics will be in excess of $20bn - can you afford to ignore this market?
The largest market is for Molecular Diagnostics, taking a 42% market share, and growing. Visiongain's new report on In Vitro Diagnostics gives you an in-depth examination of how you and your company can secure or increase your market share today. As to be expected the US dominates this market, whilst Germany has the largest market in Europe and surprisingly is the third in the world.
Nucleic Acid testing is the fastest growing market and is a key growth area. Growth in the total world market is estimated to be in the region of 7%.
Visiongain's World Market for In Vitro Diagnostics Report 2005 covers the following topics with revenues and market share by country for most applications:
- Regulation
- Molecular Technologies
- Nucleic Acid Testing
- Protein Chip Technologies
- In Vitro Diagnostics at Point of Care Use
- Personal use of In Vitro Diagnostics
- Future Use of In Vitro Diagnostics in Diabetes
- Future Use of In Vitro Diagnostics in Cancer
- In Vitro Diagnostics in Cardiac Monitoring
- Genetic Testing
- Future Markets
- Future Growth Areas
Why You Must Buy this Report?
With over 30 tables, news, insights, the latest developments, and a complete survey of the World Market for In Vitro Diagnostics. This report is a vital addition in the understanding of this lucrative and fast growing market arena. You can not afford to do without this latest report from visiongain. We look forward to receiving your order.
Table of Contents
- 1. In Vitro Diagnostics
- 1.1 Regional Markets for In Vitro Diagnostic Technologies
- 2. An Overview of the Regulatory Environment Surrounding In Vitro Diagnostics
- 2.1 How are In Vitro Diagnostic Technologies Regulated by the FDA?
- 2.2 How are IVDs Classified?
- 2.2.1 Class I - General Controls
- 2.2.2 Class II - Special Controls
- 2.2.3 Class III - Premarket Approval
- 2.3 The Regulatory Exemption of General Purpose Reagents by the FDA
- 2.4 The Regulatory Exemption of Analyte Specific Reagents by the FDA
- 2.5 The Clinical Laboratory Improvement Amendments of 1988 (CLIA)
- 2.6 CLIA Waiving and In Vitro Diagnostics
- 2.7 Premarket Notification [510(k)]
- 2.8 Substantial Equivalence
- 2.9 Who is Required to Make a 510(k) Submission?
- 2.10 When is a 510(k) is Submission Required?
- 2.11 When is 510(k) Submission Not Required?
- 2.12 The " Pre-IDE " Process for IVDs
- 2.13 The Fee Structure for 510(k) Pre-Market Notifications
- 2.14 What is the Anticipated Impact of the Introduction of the Review Fee for Medical Devices?
- 2.15 Will the MDUFMA Address the Current Limitations in the FDA Review Process for Medical Devices?
- 2.15.1 Limitations in the FDA Review Process
- 2.16 Premarket Approval (PMA)
- 2.17 Bypassing the FDA with In Vitro Diagnostics
- 2.17.1 ASRs and Home Brews
- 2.18 An Overview of ASR Regulation by the FDA
- 2.17.1Critical Requirements of ASR Regulation
- 2.19 The Benefits of an FDA Approved Status for In Vitro Diagnostic Technologies
- 2.19.1 HIV Gentoyping by Visible Genetics
- 2.19.2 PreGen-Plus by Exact Sciences
- 2.20 Will Regulatory Changes Affect ASRs and 'Home Brews' In Vitro Diagnostics?
- 2.21 A New Alternative to 510(k) Filing for Analytical IVD Technologies?
- 3.Molecular Technologies
- 3.1 The Growing Role of Molecular Technologies in the Future Healthcare Markets
- 3.2 Molecular Medicine and The Changing Face of Disease Diagnosis
- 3.3 The Developing Role of Molecular Technologies in Clinical Diagnostics
- 3.4 The Evolution of Molecular Medicine and the Role of Molecular Diagnostics in the Future of Healthcare
- 3.5 The Emerging Market for Molecular Diagnostics
- 3.6 The Growing Market for Molecular Diagnostic Technologies
- 3.7 The Growing Clinical Application of Molecular Diagnostic Technologies
- 4. In Vitro Molecular Diagnostic Technologies Approved for use in the United States
- 5. Nucleic Acid Testing
- 5.1 Nucleic Acid Testing in a Point-of-Care Scenario
- 5.2 Key Elements of Point-of-Care Nucleic Acid Testing
- 5.3 Clinical Genetic Testing
- 5.3 Therapeutic Diagnostics and Nucleic Acid Testing
- 6. Protein Chip Technologies as Diagnostic Devices
- 6.1 Protein Chip Technologies in Molecular Diagnostics
- 6.2 What are the Advantages and Limitations of Protein Chip Technologies in Clinical Diagnostics?
- 6.3 Diagnostic Applications of Protein ChipTechnologies
- 6.4 Cancer Diagnostics - The Key Field in the Future of Protein Chip Assays in Clinical Diagnosis
- 6.5 Key Companies and Technologies in Protein Chip Technologies for Clinical Diagnosis
- 6.5.1 ProteinChip by Ciphergen
- 6.5.2 The SELDI Process
- 6.5.3 The Trinectin Proteome Chip by Phylos
- 6.5.4 Microfluidic Chip-Based Immunoassays
- 6.5.5 Triage by Biosite
- 6.5.7 Tissue Microarray Technology
- 6.5.8 Molecular Diagnostics and Antigen-Antibody Interactions
- 6.6 Which System Will Lead the Way for Diagnostic Protein Chip Technologies?
- 7. In Vitro Diagnostics at the Point of Care
- 7.1 Point of Care IVD Technologies and Acute Disease
- 7.2 Point of Care IVD Technologies in Chronic Disease
- 7.3 What Hurdles Must be Overcome if Point of Care IVD Technologies are to Become Established in Primary Care
- 8. Personal Use In Vitro Diagnostic Technologies
- 8.1 Anemia
- 8.2 Bone Loss
- 8.3 Drug Side-Effect Monitoring
- 8.4 Hyperlipidemia
- 8.5 Malnutrition
- 8.6 Micronutrient Status
- 8.7 Therapeutic Drug Levels
- 9. The Future of In Vitro Diagnostic Technologies in Diabetes Testing
- 9.1 The Role of IVD Testing in Diabetes Management
- 9.1.1 Blood Glucose Testing
- 9.1.2 HbAIc Haemoglobin A1c or Glycated Haemoglobin Testing
- 9.1.3 Urinary Glucose Test
- 9.1.4 Urine test for 'Microalbuminuria'
- 9.2 Invasive or Noninvasive Glucose Monitoring?
- 9.3 Transdermal Glucose Sampling and Detection
- 9.4 Biosensor-Based Monitoring
- 9.4.1 Implantable Systems
- 9.4.2 Near Infrared Glucose Monitoring
- 9.5 Nanotechnologies in Glucose Monitoring
- 10. The Future of In Vitro Diagnostic Technologies in Cancer Diagnosis
- 10.1 The Growing Market for In Vitro Cancer Diagnostics
- 10.1.1 Rapid Diagnostics Technologies Set to Overshadow Routine Tests by 2008
- 10.1 The Growing Market for In Vitro Cancer Diagnostics
- 10.2 Cancer Diagnostics Will Lead the Market for Genetic Testing Technologies
- 10.2.1 What Will Emerge as the Dominant Technology Platforms in Cancer Screening?
- 10.3 Genetic Predisposition in Cancer and Diagnostic Opportunity
- 10.3.1 Breast Cancer and the BRCA Genes
- 10.3.2 Burkitt Lymphoma and the Myc Gene
- 10.3.3 Colon Cancer and the MSH Genes
- 10.3.4 Chronic Myeloid Leukemia and the BCR-ABL Gene
- 10.3.6 The p53 Tumor Suppressor Protein
- 11. Cardiac Monitoring and In vitro Diagnosis
- 11.1 The Global Market for Cardiac Monitoring
- 11.1.1 The High Cost of Unnecessay Cardiac Monitoring in the US
- 11.1.2 Early Diagnosis and Intervention Leads the Way to Cost Effective Therapy
- 11.1 The Global Market for Cardiac Monitoring
- 11.2 Leading IVD Technologies for Use in Cardiac Monitoring
- 11.2.1 Lactate Monitoring by Nova Medical
- 11.2.2 Multi-Disciplinary Monitoring by Datex-Ohmeda
- 11.2.3 Tissue Perfusion Monitoring by Cytometrics
- 11.2.4 Metracor Technologies and TNO Biomedical's RODA Monitor
- 12.1 Cancer Screening and Predisposition Testing Will Lead the Sector for Genetic Testing Technologies
- 12.2 US State Legislation and Genetic Testing
- 13.1 Molecular Diagnostics and the Future of the Market for IVD Technologies
- 13.2 Primary Care or Personal Use IVDs?
- 13.3 The Role of IVD Technologies in Drug Discovery
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