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  1. ARRIVE Essential - Experimental procedures‏‎ (1 revision)
  2. 1.4.2.3 Radioactivity‏‎ (1 revision)
  3. 1.4.2.5 Risks to unborn life‏‎ (1 revision)
  4. ARRIVE Essential - Randomization‏‎ (1 revision)
  5. ARRIVE Essential - Results‏‎ (1 revision)
  6. ARRIVE Essential - Sample size‏‎ (1 revision)
  7. 4.3.1.3 Revising items‏‎ (1 revision)
  8. Hauptseite‏‎ (1 revision)
  9. 2.1.1 Study (experimental) plan‏‎ (1 revision - redirect page)
  10. Implementation Strategy‏‎ (1 revision - redirect page)
  11. 1.4.3.1 Quality in collaborative research‏‎ (1 revision - redirect page)
  12. 2.4.1 Non-public reporting‏‎ (1 revision)
  13. Challenges‏‎ (1 revision)
  14. Internal assessment‏‎ (1 revision)
  15. 4.3.2.4 Deleting NEEDs‏‎ (1 revision)
  16. 4 Continuous improvement‏‎ (1 revision)
  17. 1.4.2.1 Biosafety‏‎ (1 revision)
  18. 1.5.3 Management of resources‏‎ (2 revisions)
  19. Why quality matters‏‎ (2 revisions)
  20. 1.5.2.1 Organigram‏‎ (2 revisions)
  21. 1.5.4.1 Independence of internal compliance assessment‏‎ (2 revisions)
  22. 3.4.1.7 Frequency and procedure of observation of animals‏‎ (2 revisions)
  23. 1.4.2.4 Genetically modified organisms‏‎ (2 revisions)
  24. 1.5.2.2 Management‏‎ (2 revisions)
  25. 1.5.4.2 Internal assessment of the organizations' quality professionals‏‎ (2 revisions)
  26. 3.2.1 General guidance on training‏‎ (2 revisions)
  27. 3.4.1.8 Animal health and genetic monitoring‏‎ (2 revisions)
  28. 3.4.1.9 Veterinary interventions during the study‏‎ (2 revisions)
  29. 4.2.4 Key performance indicators‏‎ (2 revisions)
  30. 1.4.2.6 Handling of controlled substances‏‎ (2 revisions)
  31. 4.3.1.1 Adding new items‏‎ (2 revisions)
  32. 1.4.2.8 Human data protection‏‎ (2 revisions)
  33. 1.5.2.6 Supporting team‏‎ (2 revisions)
  34. 3.3.1 Fit-for-purpose working environment‏‎ (2 revisions)
  35. 3.4.2.2 Antibody validation‏‎ (2 revisions)
  36. ARRIVE Essential - Statistical methods‏‎ (2 revisions)
  37. 1.3.2 Sources of pressure and bias-producing communication of pressure‏‎ (2 revisions)
  38. 3.5.1 Animal and non-animal method and assay qualification‏‎ (2 revisions)
  39. Abbreviations‏‎ (2 revisions)
  40. 1.5.3.1 Personnel‏‎ (2 revisions)
  41. 1.5.3.2 Facilities‏‎ (2 revisions)
  42. 3.4.1.11 Animal euthanasia procedures‏‎ (2 revisions)
  43. 1.5.3.3 Laboratory and experimental equipment used for measurement‏‎ (2 revisions)
  44. 1.5.3.4 Electronic information system‏‎ (2 revisions)
  45. 1.5.3.5 Organization-specific know how‏‎ (2 revisions)
  46. 1.5.3.6 Documentation requirement for sample and material‏‎ (2 revisions)
  47. 4.1.3 External Assessment‏‎ (2 revisions)
  48. ARRIVE Essential - Blinding‏‎ (2 revisions)
  49. 1.5.3.7 Retained personnel records‏‎ (2 revisions)
  50. ARRIVE Essential - Experimental animals‏‎ (2 revisions)
  51. 1.4.2.2 Chemical safety‏‎ (3 revisions)
  52. 4.2.1 Installation of solutions, actions and mitigation strategies‏‎ (3 revisions)
  53. ARRIVE Essential - Inclusion and exclusion criteria‏‎ (3 revisions)
  54. 2.2.2 Use of template for (manual) data recording‏‎ (3 revisions)
  55. 3.4.2.1 Cell culturing‏‎ (3 revisions)
  56. 1.3.1 Transparency‏‎ (3 revisions)
  57. ARRIVE Essential - Study design‏‎ (3 revisions)
  58. Information on the calculation of the priority ranking‏‎ (3 revisions)
  59. 1.3.3 Promotion criteria within a research unit‏‎ (3 revisions)
  60. 3.4.1.10 Surgical procedures‏‎ (3 revisions)
  61. 1.3.4 Performance criteria and assessment‏‎ (3 revisions)
  62. 2.4.2 Publication‏‎ (3 revisions)
  63. 3.4.1.2 Animal procurement & identification‏‎ (3 revisions)
  64. Dossier‏‎ (3 revisions)
  65. 1.4.3.4 Academia-academia: Research as collaboration‏‎ (3 revisions)
  66. 3.4.1.3 Animal housing conditions‏‎ (3 revisions)
  67. 3.4.1.4 Animal environmental conditions‏‎ (3 revisions)
  68. 3.4.1.5 Food, watering and bedding‏‎ (3 revisions)
  69. 3.4.1.6 Sanitation procedure‏‎ (4 revisions)
  70. ARRIVE Essential - Outcome measures‏‎ (4 revisions)
  71. 3.2.2 Good Research Practice training‏‎ (4 revisions)
  72. 1.5.2.4 Principal investigators and study directors‏‎ (4 revisions)
  73. 2.3.1.1 Converting non-electronic information into an electronic form‏‎ (4 revisions)
  74. 1.4.2.7 Animal care and use‏‎ (4 revisions)
  75. 1.5.2.7 Quality professionals‏‎ (4 revisions)
  76. 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use‏‎ (4 revisions)
  77. 3.4.2.3 Biological and technical replicates‏‎ (4 revisions)
  78. 1.5.2 Roles and responsibilities of involved personnel and organization‏‎ (4 revisions)
  79. 2.3.4 Data visualization‏‎ (4 revisions)
  80. 3.3.3 Management of research materials and reagents‏‎ (4 revisions)
  81. 3.5.3 Minimum reporting guidelines‏‎ (4 revisions)
  82. 2.4 Reporting‏‎ (4 revisions)
  83. 3.4.1.1 Ethical evaluation and authorization process of animal use‏‎ (4 revisions)
  84. 3 Support Processes‏‎ (4 revisions)
  85. 2.1.5 Pre-specification‏‎ (4 revisions)
  86. Risk Management Case Studies‏‎ (4 revisions)
  87. 1.4.1 Research ethics‏‎ (4 revisions)
  88. 3.1.2.2 Process for witnessing of records‏‎ (4 revisions)
  89. 2.2.1 Use of SOPs for standard experiments‏‎ (5 revisions)
  90. 3.1.3 Data security‏‎ (5 revisions)
  91. ​3.1.2.2 Process for witnessing of records‏‎ (5 revisions)
  92. 1.5.2.3 Process owner‏‎ (5 revisions)
  93. Experimental Record‏‎ (5 revisions)
  94. 1.5.5 Sustainability‏‎ (5 revisions)
  95. 1.5.2.5 Research team‏‎ (5 revisions)
  96. 2.1.10 Plausibility check‏‎ (5 revisions)
  97. 3.2.4 Training on specific methods, tasks and activities‏‎ (5 revisions)
  98. 4.3.1.2 Deleting items‏‎ (5 revisions)
  99. 2.1.2 Unique study ID‏‎ (5 revisions)
  100. 3.1.2.1 Traceability of data and any person having impact on data​‏‎ (5 revisions)

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