Open Access
Issue
MATEC Web Conf.
Volume 135, 2017
8th International Conference on Mechanical and Manufacturing Engineering 2017 (ICME’17)
Article Number 00020
Number of page(s) 10
DOI https://doi.org/10.1051/matecconf/201713500020
Published online 20 November 2017
  1. Department of Health London (2000). “An organisation with a memory - Report of an expert group on learning from adverse events in the NHS,” Clin. Med., vol. 2, no. 5, pp. 452–457. [Google Scholar]
  2. Patient Safety Observatory (2007). “Safety in doses: medication safety incidents in the NHS,” pp. 9–12. [Google Scholar]
  3. National Patient Safety Agency (2008) “Device-related incidents : reports of serious harm,” vol. 9, no. 9, pp. 2007–2009. [Google Scholar]
  4. B. Toft (2001) “External inquiry into the adverse incident that occurred at queen's medical centre, Nottingham, 4th January 2001,” Inquiry, no. January, p. 76. [Google Scholar]
  5. S. I. Panel (2007) “Report on a Medication Incident of Intrathecal Administration of Vincristine in Prince of Wales Hospital,” no. August. [Google Scholar]
  6. B. D. Franklin, S. S. Panesar, C. Vincent, and L. J. Donaldson (2014). “Identifying systems failures in the pathway to a catastrophic event: An analysis of national incident report data relating to vinca alkaloids,” BMJ Qual. Saf., vol. 23, no. 9, pp. 765–772. [CrossRef] [Google Scholar]
  7. J. L. Martin, B. J. Norris, E. Murphy, and J. a. Crowe (2008). “Medical device development: The challenge for ergonomics,” Appl. Ergon., vol. 39, no. 3, pp. 271–283. [CrossRef] [Google Scholar]
  8. A. N. Thomas, U. Panchagnula, and R. J. Taylor (2009). “Review of patient safety incidents submitted from Critical Care Units in England & Wales to the UK National Patient Safety Agency,” Anaesthesia, vol. 64, no. 11, pp. 1178–1185. [CrossRef] [Google Scholar]
  9. A. N. Thomas and B. A. McGrath (2009). “Patient safety incidents associated with airway devices in critical care: A review of reports to the UK National Patient Safety Agency,” Anaesthesia, vol. 64, no. 4, pp. 358–365. [CrossRef] [Google Scholar]
  10. A. N. Thomas and U. Panchagnula (2008) “Medication-related patient safety incidents in critical care: A review of reports to the UK National Patient Safety Agency,” Anaesthesia, vol. 63, no. 7, pp. 726–733, 2008. [CrossRef] [Google Scholar]
  11. A. N. Thomas and I. Galvin (2008). “Patient safety incidents associated with equipment in critical care: A review of reports to the UK National Patient Safety Agency,” Anaesthesia, vol. 63, no. 11, pp. 1193–1197. [CrossRef] [Google Scholar]
  12. National Patient Safety Agency (2016). “Guidance notes on National Reporting and Learning System quarterly data summary publications,” no. September. [Google Scholar]
  13. European Commission and D. G. Health (2001). “Medical Devices : Guidance document medical device software,” no. July 2001, pp. 1–21. [Google Scholar]
  14. T. M. Report (2016). “2016 Top Markets Report Medical Devices Overview and Key Findings,” pp. 1–9. [Google Scholar]
  15. W. a. Herman and G. B. Devey (2007). “Future Trends in Medical Device Technologies,” FDA Natl. Sci. Found. [Google Scholar]
  16. J. Cunningham, B. Dolan, D. Kelly, and C. Young (2015). “Medical Device Sectoral Overview,” Galw. City Cty. Econ. Ind. Baseline Study. [Google Scholar]
  17. O. M. F. De Troyer and C. J. Leune (1998). “WSDM: a user centered design method for Web sites,” Comput. Networks ISDN Syst., vol. 30, no. 1-7, pp. 85–94. [CrossRef] [Google Scholar]
  18. J. L. Martin, D. J. Clark, S. P. Morgan, J. A. Crowe, and E. Murphy (2012) “A usercentred approach to requirements elicitation in medical device development: A case study from an industry perspective,” Appl. Ergon., vol. 43, no. 1, pp. 184–190. [CrossRef] [Google Scholar]
  19. D. R. Kaufman, V. L. Patel, C. Hilliman, P. C. Morin, J. Pevzner, R. S. Weinstock, R. Goland, S. Shea, and J. Starren (2003). “Usability in the real world: Assessing medical information technologies in patients' homes,” J. Biomed. Inform., vol. 36, no. 1–2, pp. 45–60. [CrossRef] [Google Scholar]
  20. J. N. Amoore (2014). “A Structured Approach for Investigating the Causes of Medical Device Adverse Events,” vol. 2014, no. Table 1. [Google Scholar]
  21. M. Aljazzazi, M. Rawashdeh, T. Alshawaheen, and A. Malkawi (2013). “A User - Requirements Approach in Medical Devices Maintenance System Development : A Case Study from an Industry Perspective,” World Acad. Sci. Eng. Technol., vol. 75, no. 3, pp. 780–790. [Google Scholar]
  22. O. Safety (2000). “Ergonomics : The Study of Work,” vol. 2000. [Google Scholar]
  23. N. Moray (2000) “Culture, politics and ergonomics.,” Ergonomics, vol. 43, no. 7, pp. 858–868. [CrossRef] [Google Scholar]
  24. L. Fennigkoh and H. Diego (2009). “Human Factors and the Control of Medical Devi|Freescale,” pp. 39–43. [Google Scholar]
  25. J. Zhang, T. R. Johnson, V. L. Patel, D. L. Paige, and T. Kubose (2003). “Using usability heuristics to evaluate patient safety of medical devices,” J. Biomed. Inform., vol. 36, no. 1–2, pp. 23–30. [CrossRef] [Google Scholar]
  26. J. Horsky, J. Zhang, and V. L. Patel (2005). “To err is not entirely human:Complex technology and user cognition,” J. Biomed. Inform., vol. 38, no. 4, pp. 264–266. [CrossRef] [Google Scholar]
  27. S. F. Liu, Y. Lee, and Y. Huang (2009). “A brief fatigue inventory of shoulder health developed by quality function deployment technique,” J. Shoulder Elb. Surg., vol. 18, no. 3, pp. 418–423. [CrossRef] [Google Scholar]
  28. A. Kianfar and F. Kianfar (2010) “Plant function deployment via RCM and QFD,” J. Qual. Maint. Eng., vol. 16, no. 4, pp. 354–366. [CrossRef] [Google Scholar]
  29. P. Buckle, P. J. Clarkson, R. Coleman, J. Bound, J. Ward, and J. Brown (2010) “Systems mapping workshops and their role in understanding medication errors in healthcare,” Appl. Ergon., vol. 41, no. 5, pp. 645–656. [CrossRef] [Google Scholar]
  30. P. Buckle, P. J. Clarkson, R. Coleman, J. Ward, and J. Anderson (2006). “Patient safety, systems design and ergonomics,” Appl. Ergon., vol. 37, no. 4 SPEC. ISS., pp. 491–500. [CrossRef] [Google Scholar]
  31. N. Khambete and A. Murray (2012). “National efforts to improve healthcare technology management and medical device safety in india,” pp. 1–5. [Google Scholar]
  32. Department of Health (2003). “A System-wide Design-led Approach (Design for Patient Safety),” Design, p. 45. [Google Scholar]
  33. de Laveaga and Adam E. (2012) “An Investigation Of Medical Device Design And Physical Ergonomics In Healthcare,” Industrial and Management Systems Engineering - Dissertations and Student Research., Paper 32. [Google Scholar]
  34. P. Carayon and K. E. Wood (2010). “Patient safety: The role of human factors and systems engineering,” Stud. Health Technol. Inform., vol. 153, pp. 23–46. [Google Scholar]
  35. L. Lin, K. J. Vicente, and D. J. J. Doyle (2001). “Patient Safety, Potential Adverse Drug Events, and Medical Device Design: A Human Factors Engineering Approach,” J. Biomed. Inform., vol. 34, no. 4, pp. 274–84. [CrossRef] [Google Scholar]
  36. A. Çetin (2004). “Applying Product Design Methods to Medical Device Design With a Case Study on Home Care Devices,” Strategy. [Google Scholar]
  37. L. Duque-Muñoz, C. A. Aguirre-Echeverry, and G. Castellanos- Domínguez (2014). “EEG rhythm analysis using stochastic relevance,” IFMBE Proc., vol. 41, pp. 658–661. [CrossRef] [Google Scholar]
  38. H. Care (2012). “2012 Symposium on Human Factors and Ergonomics,”. [Google Scholar]
  39. The Association for Packaging and Processing Technologies (2016). “Pharmaceutical & Medical Devices: Trends and Opportunities in Packaging Operations,”. [Google Scholar]
  40. N. Radhadevi, V. Balamuralidhara, T. M. P. Kumar, and V. Ravi (2012). “Regulatory guidelines for medical devices in India: An overview,” Asian J. Pharm., vol. 6, no. 1, pp. 10–17. [CrossRef] [Google Scholar]
  41. M. Mutingi, P. Dube, and C. Mbohwa (2017) “A Modular Product Design Approach for Sustainable Manufacturing in A Fuzzy Environment,” Procedia Manuf., vol. 8, no. October 2016, pp. 471–478. [CrossRef] [Google Scholar]
  42. J. E. Brown, R. Qiang, P. J. Stadnik, S. Member, L. J. Stotts, S. Member, and J. A. Von Arx (2016).“MR Conditional Safety Assessment of Implanted Medical Devices : Advantages of Computational Human Phantoms,” pp. 6465–6468. [Google Scholar]
  43. National Patient Safety Agency (2010). “Design for Patient Safety User testing in the development of medical devices,” Patient Safety, 2nd Ed., p. 68. [Google Scholar]
  44. S. Weininger and D. Ph (2009). “and Its Relationship to Safety and Effectiveness,” Pace Pacing Clin. Electrophysiol.. [Google Scholar]
  45. J. Park, C. Yi, K. Kwon, and J. W. Jeon (2014). “Method Of Fault Injection for Medical Device Based on ISO 26262,” pp. 1–2. [Google Scholar]
  46. L. Eisner (2006) “Iec 60601-1 - the Third Edition,” Regulation, pp. 8–17. [Google Scholar]
  47. Taylor A. (2013) “Standards : Medical Devices,” pp. 1–3. [Google Scholar]
  48. Mitch Gaudyn (2012). “The third edition of IEC 60601-1-A manufacturer's perspective,” no. February. [Google Scholar]
  49. J. O. Hare (2006) “Today's Moves Towards Eco-innovation in the Medical Electronics Sector,” pp. 1–10. [Google Scholar]
  50. P. G. Rajendra K. Songara, Ganesh N. Sharma, Vipul K. Gupta (2010). “Need For Harmonization Of Labeling Of Medical Devices: A Review,” J. Adv. Pharm. Teachnology, vol. 1, no. 2, pp. 1–36. [Google Scholar]
  51. Rigel Medical (2007). “A Practical Guide to IEC 60601-1,”. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.