arcoro – GLOSSAR

In our arcoro glossary, we explain the most important terms from the field of medical technology & pharmaceuticals. For companies. For candidates. From Active Implantable Medical Device (AIMD) to Clinical Affairs and Medical Device Regulation (MDR) to vigilance systems. Short, compact and comprehensible – 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 Centre for Disease Prevention and Control (ECDC)
  39. European Database on Medical Devices (EUDAMED)
  40. European Medicines Agency (EMA)
  41. Exoskeleton
  42. Failure Mode and Effect Analysis (FMEA)
  43. Federal Institute for Drugs and Medical Devices
  44. Federal Ministry of Health (BMG)
  45. Foil sensor technology
  46. Food and Drug Administration (FDA)
  47. Generic drugs
  48. German Medicines Act (AMG)
  49. Glucose
  50. Good Distribution Practice (GDP)
  51. Good Manufacturing Practice (GMP)
  52. Head Mounted Display
  53. Health Wearables
  54. Hearing loss
  55. Heart attack
  56. IEC 62304
  57. Implant
  58. Implant ID card
  59. Insulin
  60. International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH)
  61. Internet of Medical Things (IoMT)
  62. Invasive products
  63. ISO standards
  64. Laboratory diagnostics
  65. Medical Device Regulation (MDR)
  66. Medical Devices
  67. Medical Robotics
  68. Medical technology
  69. Miniaturization
  70. Multi-organ failure
  71. Narcotics Act
  72. National Working Group (NAKI)
  73. non-interventional study (NIS)
  74. Orthosis
  75. Pharmaceutical industry
  76. Pharmaceutical Trade Regulation
  77. Pharmacopoeia
  78. Pharmacovigilance
  79. Pivotal study
  80. Placebo
  81. Placebo effect
  82. Post Market Surveillance (PMS)
  83. Preclinical studies
  84. prosthesis
  85. prosthetics
  86. Psychosomatic diseases
  87. Quality of supply
  88. Quality records
  89. Reanimation
  90. Regulatory Affairs
  91. Rehabilitation
  92. Side effect
  93. Single-blind study
  94. Sleep analysis
  95. Smart Textiles
  96. stroke
  97. Surgery
  98. Telemedicine
  99. Tremor
  100. UL 2900-2-1
  101. Unique Device Identification System (UDI)
  102. Verum
  103. Vigilance system
  104. vital parameters
  105. World Health Organization (WHO)
Unfortunately, there is no entry in the glossary for this search combination yet.

arcoro CONTACT

Contact person for project and network inquiries

Our contact persons are available at all times to answer any questions you may have about the market and our range of services. We look forward to hearing from you.

More contact options