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Showing below up to 100 results in range #51 to #150.

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  1. 3.1.1 Platform to record data‏‎ (17:34, 5 September 2020)
  2. 3.1.2.1 Traceability of data and any person having impact on data​‏‎ (17:36, 5 September 2020)
  3. ​3.1.2.2 Process for witnessing of records‏‎ (17:37, 5 September 2020)
  4. 3.2.1 General guidance on training‏‎ (18:26, 5 September 2020)
  5. 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use‏‎ (18:28, 5 September 2020)
  6. 3.3.3 Management of research materials and reagents‏‎ (18:29, 5 September 2020)
  7. 3.4.1.2 Animal procurement & identification‏‎ (18:33, 5 September 2020)
  8. 3.4.1.3 Animal housing conditions‏‎ (18:34, 5 September 2020)
  9. 3.4.1.4 Animal environmental conditions‏‎ (18:34, 5 September 2020)
  10. 3.4.1.5 Food, watering and bedding‏‎ (18:35, 5 September 2020)
  11. 3.4.1.6 Sanitation procedure‏‎ (18:35, 5 September 2020)
  12. 3.4.1.7 Frequency and procedure of observation of animals‏‎ (18:35, 5 September 2020)
  13. 3.4.1.8 Animal health and genetic monitoring‏‎ (18:36, 5 September 2020)
  14. 3.4.1.9 Veterinary interventions during the study‏‎ (18:36, 5 September 2020)
  15. 3.4.1.10 Surgical procedures‏‎ (18:37, 5 September 2020)
  16. 3.4.1.11 Animal euthanasia procedures‏‎ (18:37, 5 September 2020)
  17. 3.4.2.1 Cell culturing‏‎ (18:38, 5 September 2020)
  18. 3.5.1 Animal and non-animal method and assay qualification‏‎ (18:39, 5 September 2020)
  19. Examples for Errors‏‎ (19:08, 5 September 2020)
  20. 4.2.4 Key performance indicators‏‎ (19:20, 5 September 2020)
  21. 4.3.1.1 Adding new items‏‎ (19:20, 5 September 2020)
  22. ARRIVE 2.0‏‎ (09:36, 29 September 2020)
  23. 3.4.1 Animal characteristics, care and use‏‎ (10:15, 29 September 2020)
  24. 3.4.1.1 Ethical evaluation and authorization process of animal use‏‎ (09:22, 1 October 2020)
  25. PREPARE‏‎ (14:42, 2 October 2020)
  26. 4.2.3 Responsible conduct of research‏‎ (15:36, 3 November 2020)
  27. 3.1.3 Data security‏‎ (08:18, 9 November 2020)
  28. 3.4.2.2 Antibody validation‏‎ (12:07, 24 November 2020)
  29. 3.2.4 Training on specific methods, tasks and activities‏‎ (10:45, 8 December 2020)
  30. 3.4.2.3 Biological and technical replicates‏‎ (16:48, 3 February 2021)
  31. 3.1.2 Procedures for how and when to record data‏‎ (09:01, 12 February 2021)
  32. 1.3.1 Transparency‏‎ (10:21, 15 February 2021)
  33. 1.5.1 Quality policy‏‎ (10:23, 15 February 2021)
  34. 1.5.2.3 Process owner‏‎ (10:24, 15 February 2021)
  35. 1.5.4 Prevention of Conflict of Interest‏‎ (10:25, 15 February 2021)
  36. 3.1.2.2 Process for witnessing of records‏‎ (10:29, 15 February 2021)
  37. 4.3.1.2 Deleting items‏‎ (09:53, 22 February 2021)
  38. 2.1.8 Randomisation‏‎ (07:34, 4 March 2021)
  39. 2.3.1.1 Converting non-electronic information into an electronic form‏‎ (09:31, 10 March 2021)
  40. EQIPD principles‏‎ (09:14, 16 March 2021)
  41. Performance Standards‏‎ (09:18, 18 March 2021)
  42. FAQ‏‎ (19:40, 23 March 2021)
  43. 2.3.4 Data visualization‏‎ (19:41, 23 March 2021)
  44. 2.3.3 Statistical analysis‏‎ (19:41, 23 March 2021)
  45. 2.1.10 Plausibility check‏‎ (19:43, 23 March 2021)
  46. 2.1.7 Blinding‏‎ (19:43, 23 March 2021)
  47. 1.5.2.7 Quality professionals‏‎ (19:46, 23 March 2021)
  48. 1.5.2.5 Research team‏‎ (19:47, 23 March 2021)
  49. 2.1.3 Appraisal of literature and systematic reviews‏‎ (12:43, 24 March 2021)
  50. 2.1.9 Inclusion and exclusion criteria‏‎ (12:46, 24 March 2021)
  51. 2.4 Reporting‏‎ (12:47, 24 March 2021)
  52. 1.5.2.4 Principal investigators and study directors‏‎ (12:54, 24 March 2021)
  53. ARRIVE Essential - Outcome measures‏‎ (13:02, 24 March 2021)
  54. 2.1.5 Pre-specification‏‎ (13:03, 24 March 2021)
  55. 1.4.3 Quality in collaborative research‏‎ (06:38, 25 March 2021)
  56. 4.3.2 Using the EQIPD applications‏‎ (16:51, 29 March 2021)
  57. 4.3.2.2 Creating NEEDs‏‎ (16:53, 29 March 2021)
  58. 4.3.2.3 Revising NEEDs‏‎ (12:47, 31 March 2021)
  59. 1.1 Mission‏‎ (16:04, 7 April 2021)
  60. 1.5.2 Roles and responsibilities of involved personnel and organization‏‎ (09:23, 9 April 2021)
  61. EQIPD for Core Facilities‏‎ (12:39, 15 April 2021)
  62. 2.3.2 Primary analysis and evaluation of raw data‏‎ (13:17, 15 April 2021)
  63. 2.2.3 Documentation of the experiment and deviations‏‎ (13:27, 15 April 2021)
  64. 1.2 Scope‏‎ (06:44, 20 April 2021)
  65. 2.1.2 Unique study ID‏‎ (07:51, 28 April 2021)
  66. Examples of implementing a unique study ID‏‎ (07:51, 29 April 2021)
  67. Documentation in EQIPD‏‎ (08:49, 6 May 2021)
  68. 1.4.2 Adherence to legal and regulatory considerations‏‎ (06:45, 7 May 2021)
  69. Core Requirements‏‎ (17:55, 10 May 2021)
  70. Experimental Record‏‎ (18:22, 10 May 2021)
  71. 4.3.2.1 Using the Planning Tool‏‎ (07:50, 14 May 2021)
  72. 3.2.3 Implementation of the EQIPD Quality System‏‎ (07:50, 14 May 2021)
  73. NEED‏‎ (08:38, 20 May 2021)
  74. Why quality matters‏‎ (12:37, 9 June 2021)
  75. 1.4.3.2 Industry-academia: Research as collaboration‏‎ (09:46, 14 June 2021)
  76. 4.2.1 Installation of solutions, actions and mitigation strategies‏‎ (08:16, 24 June 2021)
  77. 1.4.3.3 Academia-academia: Research as service‏‎ (08:18, 25 June 2021)
  78. 3.2.2 Good Research Practice training‏‎ (10:57, 26 July 2021)
  79. 4.1.2 Self assessment‏‎ (12:12, 13 August 2021)
  80. Spot checks‏‎ (11:52, 16 August 2021)
  81. 2.1.6 Sample size and power analysis‏‎ (07:43, 14 September 2021)
  82. 2.3.1 Generation, recording, handling and archiving of raw data‏‎ (09:29, 20 September 2021)
  83. 4.1.3 External assessment‏‎ (11:11, 20 September 2021)
  84. 1.4.1.2 Data sharing‏‎ (05:47, 6 October 2021)
  85. 1.3.5 Reward system and incentives‏‎ (05:50, 6 October 2021)
  86. 2.1.11 Preregistration‏‎ (05:57, 6 October 2021)
  87. 2.1.1 Study protocol‏‎ (12:24, 20 October 2021)
  88. 4.1.1 Risk assessment‏‎ (12:36, 20 October 2021)
  89. 2.2.1 Use of SOPs for standard experiments‏‎ (17:27, 25 October 2021)
  90. 1.5.5 Sustainability‏‎ (12:26, 26 October 2021)
  91. Glossary‏‎ (08:26, 2 November 2021)
  92. 4.2.2 Error and incident management‏‎ (08:06, 11 November 2021)
  93. 1.4.3.4 Academia-academia: Research as collaboration‏‎ (09:40, 16 November 2021)
  94. 1.4.3.1 Industry-academia: Research as service‏‎ (09:59, 16 November 2021)
  95. 2.1.4 Purpose of research‏‎ (16:53, 15 December 2021)
  96. 1.4.3.5 Expectations from public funders‏‎ (14:13, 2 February 2023)
  97. Risk Management Case Studies‏‎ (08:42, 11 April 2023)
  98. 3.5.2 Protocols for methods and assays‏‎ (12:25, 15 June 2023)
  99. 3.5.3 Minimum reporting guidelines‏‎ (12:35, 15 June 2023)
  100. 3.1.2.1 Traceability of data and any person having impact on data‏‎ (11:01, 20 September 2023)

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