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  1. 3.2.3 Implementation of the EQIPD Quality System‏‎ (80 revisions)
  2. 1.4.3.3 Academia-academia: Research as service‏‎ (51 revisions)
  3. Core Requirements‏‎ (50 revisions)
  4. Documentation in EQIPD‏‎ (49 revisions)
  5. EQIPD Quality System‏‎ (44 revisions)
  6. 2.1.6 Sample size and power analysis‏‎ (41 revisions)
  7. Toolbox‏‎ (39 revisions)
  8. 4.3.2.1 Using the Planning Tool‏‎ (32 revisions)
  9. PREPARE‏‎ (28 revisions)
  10. 2.1.4 Purpose of research‏‎ (27 revisions)
  11. Glossary‏‎ (26 revisions)
  12. 1.1 Mission‏‎ (25 revisions)
  13. EQIPD for Core Facilities‏‎ (25 revisions)
  14. 4.3.2.2 Creating NEEDs‏‎ (24 revisions)
  15. 2.1.11 Preregistration‏‎ (23 revisions)
  16. NEED‏‎ (23 revisions)
  17. 2.1.7 Blinding‏‎ (23 revisions)
  18. 4.3.2 Using the EQIPD applications‏‎ (18 revisions)
  19. 1.4.3 Quality in collaborative research‏‎ (18 revisions)
  20. 4.2.2 Error and incident management‏‎ (17 revisions)
  21. 4.1.3 External assessment‏‎ (17 revisions)
  22. Examples of implementing a unique study ID‏‎ (16 revisions)
  23. 2.1.1 Study protocol‏‎ (15 revisions)
  24. 3.1.2.1 Traceability of data and any person having impact on data‏‎ (15 revisions)
  25. 1.4.3.2 Industry-academia: Research as collaboration‏‎ (14 revisions)
  26. 2.1.8 Randomisation‏‎ (14 revisions)
  27. 1.5.4 Prevention of Conflict of Interest‏‎ (13 revisions)
  28. 4.3.2.3 Revising NEEDs‏‎ (13 revisions)
  29. 4.1.1 Risk assessment‏‎ (13 revisions)
  30. ARRIVE 2.0‏‎ (13 revisions)
  31. 1.4.3.5 Expectations from public funders‏‎ (13 revisions)
  32. 2.3.3 Statistical analysis‏‎ (12 revisions)
  33. 3.5.2 Protocols for methods and assays‏‎ (12 revisions)
  34. 4.1.2 Self assessment‏‎ (12 revisions)
  35. 1.4.1.2 Data sharing‏‎ (12 revisions)
  36. EQIPD principles‏‎ (11 revisions)
  37. 1.2 Scope‏‎ (11 revisions)
  38. FAQ‏‎ (10 revisions)
  39. 2.3.1 Generation, recording, handling and archiving of raw data‏‎ (10 revisions)
  40. 1.4.2 Adherence to legal and regulatory considerations‏‎ (10 revisions)
  41. EQIPD‏‎ (10 revisions)
  42. 3.4.1 Animal characteristics, care and use‏‎ (9 revisions)
  43. 1.4.3.1 Industry-academia: Research as service‏‎ (9 revisions)
  44. Performance Standards‏‎ (9 revisions)
  45. 2.1.3 Appraisal of literature and systematic reviews‏‎ (8 revisions)
  46. 1.4.3.2 Quality in collaborative research‏‎ (8 revisions)
  47. 3.1.2 Procedures for how and when to record data‏‎ (7 revisions)
  48. 1.5.1 Quality policy‏‎ (7 revisions)
  49. Examples for Errors‏‎ (7 revisions)
  50. 2.2.3 Documentation of the experiment and deviations‏‎ (7 revisions)
  51. 2.3.2 Primary analysis and evaluation of raw data‏‎ (7 revisions)
  52. 1.3.5 Reward system and incentives‏‎ (7 revisions)
  53. 3.1.1 Platform to record data‏‎ (7 revisions)
  54. 2.1.9 Inclusion and exclusion criteria‏‎ (6 revisions)
  55. 4.2.3 Responsible conduct of research‏‎ (6 revisions)
  56. 1.4.1.1 Research integrity‏‎ (6 revisions)
  57. Spot checks‏‎ (6 revisions)
  58. 2.2.1 Use of SOPs for standard experiments‏‎ (5 revisions)
  59. 3.1.3 Data security‏‎ (5 revisions)
  60. ​3.1.2.2 Process for witnessing of records‏‎ (5 revisions)
  61. Experimental Record‏‎ (5 revisions)
  62. 1.5.2.3 Process owner‏‎ (5 revisions)
  63. 1.5.5 Sustainability‏‎ (5 revisions)
  64. 3.2.4 Training on specific methods, tasks and activities‏‎ (5 revisions)
  65. 4.3.1.2 Deleting items‏‎ (5 revisions)
  66. 1.5.2.5 Research team‏‎ (5 revisions)
  67. 2.1.10 Plausibility check‏‎ (5 revisions)
  68. 2.1.2 Unique study ID‏‎ (5 revisions)
  69. 3.1.2.1 Traceability of data and any person having impact on data​‏‎ (5 revisions)
  70. 3.4.1.6 Sanitation procedure‏‎ (4 revisions)
  71. ARRIVE Essential - Outcome measures‏‎ (4 revisions)
  72. 3.2.2 Good Research Practice training‏‎ (4 revisions)
  73. 2.3.1.1 Converting non-electronic information into an electronic form‏‎ (4 revisions)
  74. 1.5.2.4 Principal investigators and study directors‏‎ (4 revisions)
  75. 1.4.2.7 Animal care and use‏‎ (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. 1.5.2.7 Quality professionals‏‎ (4 revisions)
  79. 2.3.4 Data visualization‏‎ (4 revisions)
  80. 3.3.3 Management of research materials and reagents‏‎ (4 revisions)
  81. 1.5.2 Roles and responsibilities of involved personnel and organization‏‎ (4 revisions)
  82. 3.5.3 Minimum reporting guidelines‏‎ (4 revisions)
  83. 2.4 Reporting‏‎ (4 revisions)
  84. 3.4.1.1 Ethical evaluation and authorization process of animal use‏‎ (4 revisions)
  85. 3 Support Processes‏‎ (4 revisions)
  86. 2.1.5 Pre-specification‏‎ (4 revisions)
  87. Risk Management Case Studies‏‎ (4 revisions)
  88. 1.4.1 Research ethics‏‎ (4 revisions)
  89. 3.1.2.2 Process for witnessing of records‏‎ (4 revisions)
  90. 4.2.1 Installation of solutions, actions and mitigation strategies‏‎ (3 revisions)
  91. 1.4.2.2 Chemical safety‏‎ (3 revisions)
  92. ARRIVE Essential - Inclusion and exclusion criteria‏‎ (3 revisions)
  93. 2.2.2 Use of template for (manual) data recording‏‎ (3 revisions)
  94. 3.4.2.1 Cell culturing‏‎ (3 revisions)
  95. ARRIVE Essential - Study design‏‎ (3 revisions)
  96. 1.3.1 Transparency‏‎ (3 revisions)
  97. Information on the calculation of the priority ranking‏‎ (3 revisions)
  98. 3.4.1.10 Surgical procedures‏‎ (3 revisions)
  99. 1.3.3 Promotion criteria within a research unit‏‎ (3 revisions)
  100. 2.4.2 Publication‏‎ (3 revisions)

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