Introduction to Medical Devices: Volume 2
This Book by LIMSbook.com is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.
Table of Contents
- Chapter: 5.2 Medical Device-Related Terminology - Part 2
- Health and Information Technology
- Biomedical equipment technician
- Chief medical informatics officer
- Clinical engineering
- Computer-aided diagnosis
- Computer-aided simple triage
- Health technology
- Health technology assessment
- In silico medicine
- Medical device connectivity
- Medical image computing
- Medical technology assessment
- Telemedicine
- Design, Manufacturing, and Distribution
- 3D bioprinting
- 3D printing
- Bioburden testing
- Biomedical engineering
- Direct metal laser sintering
- Electron beam additive manufacturing
- Lattice structure
- Medical device manufacturing
- Medical logistics
- Metallic microlattice
- Microextrusion
- Package testing
- Polymer solution casting
- Reliability engineering
- Safety engineering
- Sintering
- Software of unknown pedigree
- Software reliability testing
- Stereolithography
- Sterility assurance level
- Chapter: 6. Regulatory Considerations
- 21 CFR Part 11
- Center for Devices and Radiological Health
- Central Drugs Standard Control Organization
- China Food and Drug Administration
- Design controls
- Design history file
- Federal Food, Drug, and Cosmetic Act
- Food and Drug Administration Amendments Act of 2007
- Food and Drug Administration Modernization Act of 1997
- Food and Drug Administration
- Global Harmonization Task Force
- Global Medical Device Nomenclature
- Humanitarian Device Exemption
- IEC 60601
- IEC 62304
- IEC 62366
- ISO 10993
- ISO 13485
- ISO 14155
- ISO 14971
- ISO/IEEE 11073
- ISO/TC 215
- Italian Device Registration
- Medical Device Radiocommunications Service
- Medical Device Regulation Act
- Medical device reporting
- Medical Devices Directive
- Medicines and Healthcare Products Regulatory Agency
- Medsafe
- MedWatch
- Ministry of Food and Drug Safety
- Notified body
- Office of Global Regulatory Operations and Policy
- Pharmaceuticals and Medical Devices Agency
- Postmarketing surveillance
- QSIT
- Regulation of therapeutic goods
- Regulatory affairs
- Safe Medical Device Amendments of 1990
- Therapeutic Goods Administration
- Therapeutic Products Directorate
- Type approval
- Chapter: 7. Resources
- Representative manufacturers
- 3M Health Care Ltd.
- Abbott Laboratories, Inc.
- Alcon, Inc.
- B. Braun Melsungen AG
- Baxter International, Inc.
- Bayer AG
- Becton, Dickinson and Company
- Boston Scientific Corporation
- Cardinal Health, Inc.
- Danaher Corporation
- Essilor International SA
- Fresenius SE & Co. KGaA
- GE Healthcare
- Getinge AB
- Hansen Medical, Inc.
- Intuitive Surgical, Inc.
- Johnson & Johnson, Inc.
- Medtronic PLC
- Olympus Corporation
- Philips Healthcare
- Siemens Healthcare GmbH
- Smith & Nephew PLC
- St. Jude Medical, Inc.
- Stryker Corporation
- Zimmer Biomet Holdings, Inc.
- Organizations
- AdvaMed
- Association for the Advancement of Medical Instrumentation
- Canadian Medical and Biological Engineering Society
- COCIR
- International Medical Equipment Collaborative
- MedTech Europe
- Publications and awards
- Expert Review of Medical Devices
- Journal of Medical Marketing
- MD&DI
- Medical & Biological Engineering & Computing
- Medical Design Excellence Awards
