arcoro Glossary

In our Arcoro glossary we explain the most important terms from the field of medical technology. For companies. For candidates. From Active Implantable Medical Device (AIMD) to Clinical Affairs and Medical Device Regulation (MDR) to vigilance system. Short, compact and understandable – for reading in, refreshing or as a quick knowledge to go.

Glossary

  1. 3D printing
  2. Active Implantable Medical Device (AIMD)
  3. Active Substance Master File (ASMF)
  4. Additive manufacturing
  5. Amputation
  6. Anatomical Therapeutic Chemical Code
  7. Bioequivalence Study
  8. Biohybrid materials
  9. biopsy
  10. Biotechnology
  11. Body cell
  12. Bronchial asthma
  13. Cardiovascular arrest
  14. CE-marking
  15. CENELEC
  16. chronic diseases
  17. Clinical Affairs
  18. Clinical Investigation Plan (CIP)
  19. Clinical study
  20. Continuous Glucose Monitoring (CGM)
  21. Corrective and Preventive Action (CAPA)
  22. Defibrillation
  23. Dementia
  24. Depression
  25. Diabetes mellitius
  26. Digital consultation
  27. Digital Health
  28. DIN EN ISO 13485
  29. DIN EN ISO 14155:2020
  30. DIN EN ISO 22870
  31. DIN EN ISO 9001
  32. DNA
  33. Double-Blind Study
  34. Electrocardiogram (ECG)
  35. Electronic Data Capture (EDC)
  36. Electrotherapy
  37. Ethics Committee
  38. European Database on Medical Devices (EUDAMED)
  39. Exoskeleton
  40. Failure Mode and Effect Analysis (FMEA)
  41. Federal Institute for Drugs and Medical Devices
  42. Federal Ministry of Health (BMG)
  43. Foil sensor technology
  44. Food and Drug Administration (FDA)
  45. Generic drugs
  46. German Medicines Act (AMG)
  47. Glucose
  48. Good Distribution Practice (GDP)
  49. Good Manufacturing Practice (GMP)
  50. Head Mounted Display
  51. Health Wearables
  52. Hearing loss
  53. Heart attack
  54. IEC 62304
  55. Implant
  56. Implant ID card
  57. Insulin
  58. Internet of Medical Things (IoMT)
  59. Invasive products
  60. ISO standards
  61. Laboratory diagnostics
  62. Medical Device Regulation (MDR)
  63. Medical Devices
  64. Medical Robotics
  65. Medical technology
  66. Miniaturization
  67. Multi-organ failure
  68. Narcotics Act
  69. National Working Group (NAKI)
  70. non-interventional study (NIS)
  71. Orthosis
  72. Pharmaceutical Trade Regulation
  73. Pharmacopoeia
  74. Pivotal study
  75. Placebo
  76. Placebo effect
  77. Post Market Surveillance (PMS)
  78. Preclinical studies
  79. prosthesis
  80. prosthetics
  81. Psychosomatic diseases
  82. Quality of supply
  83. Quality records
  84. Reanimation
  85. Regulatory Affairs
  86. Rehabilitation
  87. Side effect
  88. Single-blind study
  89. Sleep analysis
  90. Smart Textiles
  91. stroke
  92. Surgery
  93. Telemedicine
  94. Tremor
  95. UL 2900-2-1
  96. Unique Device Identification System (UDI)
  97. Verum
  98. Vigilance system
  99. vital parameters
  100. World Health Organization (WHO)
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