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- 3.1.2.1 Traceability of data and any person having impact on data (17:36, 5 September 2020)
- 3.1.2.2 Process for witnessing of records (17:37, 5 September 2020)
- 3.2.1 General guidance on training (18:26, 5 September 2020)
- 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use (18:28, 5 September 2020)
- 3.3.3 Management of research materials and reagents (18:29, 5 September 2020)
- 3.4.1.2 Animal procurement & identification (18:33, 5 September 2020)
- 3.4.1.3 Animal housing conditions (18:34, 5 September 2020)
- 3.4.1.4 Animal environmental conditions (18:34, 5 September 2020)
- 3.4.1.5 Food, watering and bedding (18:35, 5 September 2020)
- 3.4.1.6 Sanitation procedure (18:35, 5 September 2020)
- 3.4.1.7 Frequency and procedure of observation of animals (18:35, 5 September 2020)
- 3.4.1.8 Animal health and genetic monitoring (18:36, 5 September 2020)
- 3.4.1.9 Veterinary interventions during the study (18:36, 5 September 2020)
- 3.4.1.10 Surgical procedures (18:37, 5 September 2020)
- 3.4.1.11 Animal euthanasia procedures (18:37, 5 September 2020)
- 3.4.2.1 Cell culturing (18:38, 5 September 2020)
- 3.5.1 Animal and non-animal method and assay qualification (18:39, 5 September 2020)
- Examples for Errors (19:08, 5 September 2020)
- 4.2.4 Key performance indicators (19:20, 5 September 2020)
- 4.3.1.1 Adding new items (19:20, 5 September 2020)
- ARRIVE 2.0 (09:36, 29 September 2020)
- 3.4.1 Animal characteristics, care and use (10:15, 29 September 2020)
- 3.4.1.1 Ethical evaluation and authorization process of animal use (09:22, 1 October 2020)
- PREPARE (14:42, 2 October 2020)
- 4.2.3 Responsible conduct of research (15:36, 3 November 2020)
- 3.1.3 Data security (08:18, 9 November 2020)
- 3.4.2.2 Antibody validation (12:07, 24 November 2020)
- 3.2.4 Training on specific methods, tasks and activities (10:45, 8 December 2020)
- 3.4.2.3 Biological and technical replicates (16:48, 3 February 2021)
- 3.1.2 Procedures for how and when to record data (09:01, 12 February 2021)
- 1.3.1 Transparency (10:21, 15 February 2021)
- 1.5.1 Quality policy (10:23, 15 February 2021)
- 1.5.2.3 Process owner (10:24, 15 February 2021)
- 1.5.4 Prevention of Conflict of Interest (10:25, 15 February 2021)
- 3.1.2.2 Process for witnessing of records (10:29, 15 February 2021)
- 4.3.1.2 Deleting items (09:53, 22 February 2021)
- 2.1.8 Randomisation (07:34, 4 March 2021)
- 2.3.1.1 Converting non-electronic information into an electronic form (09:31, 10 March 2021)
- EQIPD principles (09:14, 16 March 2021)
- Performance Standards (09:18, 18 March 2021)
- FAQ (19:40, 23 March 2021)
- 2.3.4 Data visualization (19:41, 23 March 2021)
- 2.3.3 Statistical analysis (19:41, 23 March 2021)
- 2.1.10 Plausibility check (19:43, 23 March 2021)
- 2.1.7 Blinding (19:43, 23 March 2021)
- 1.5.2.7 Quality professionals (19:46, 23 March 2021)
- 1.5.2.5 Research team (19:47, 23 March 2021)
- 2.1.3 Appraisal of literature and systematic reviews (12:43, 24 March 2021)
- 2.1.9 Inclusion and exclusion criteria (12:46, 24 March 2021)
- 2.4 Reporting (12:47, 24 March 2021)