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- Hauptseite (09:05, 1 September 2020)
- 1.4.2.1 Biosafety (11:44, 1 September 2020)
- 1.4.2.3 Radioactivity (11:45, 1 September 2020)
- 1.4.2.5 Risks to unborn life (11:48, 1 September 2020)
- 1.4.2.6 Handling of controlled substances (12:08, 1 September 2020)
- 2.4.1 Non-public reporting (15:58, 2 September 2020)
- 2.4.2 Publication (16:36, 2 September 2020)
- 3.3.1 Fit-for-purpose working environment (08:42, 3 September 2020)
- 4.1.3 External Assessment (10:51, 3 September 2020)
- Dossier (13:55, 3 September 2020)
- Challenges (13:56, 3 September 2020)
- 4.3.2.4 Deleting NEEDs (14:02, 3 September 2020)
- 3 Support Processes (14:12, 3 September 2020)
- 4 Continuous improvement (14:50, 3 September 2020)
- Internal assessment (14:55, 3 September 2020)
- 4.3.1.3 Revising items (14:59, 3 September 2020)
- Information on the calculation of the priority ranking (15:02, 3 September 2020)
- 1.3.2 Sources of pressure and bias-producing communication of pressure (12:12, 5 September 2020)
- 1.3.3 Promotion criteria within a research unit (12:13, 5 September 2020)
- 1.4.1 Research ethics (12:20, 5 September 2020)
- 1.3.4 Performance criteria and assessment (12:20, 5 September 2020)
- 1.4.1.1 Research integrity (12:24, 5 September 2020)
- 1.4.2.2 Chemical safety (12:28, 5 September 2020)
- 1.4.2.4 Genetically modified organisms (12:28, 5 September 2020)
- 1.4.2.7 Animal care and use (12:29, 5 September 2020)
- 1.4.2.8 Human data protection (12:30, 5 September 2020)
- 1.5.2.1 Organigram (12:33, 5 September 2020)
- 1.5.2.2 Management (12:34, 5 September 2020)
- 1.5.2.6 Supporting team (12:36, 5 September 2020)
- 1.5.3 Management of resources (12:38, 5 September 2020)
- 1.5.3.1 Personnel (12:38, 5 September 2020)
- 1.5.3.2 Facilities (12:38, 5 September 2020)
- 1.5.3.3 Laboratory and experimental equipment used for measurement (12:39, 5 September 2020)
- 1.5.3.4 Electronic information system (12:39, 5 September 2020)
- 1.5.3.5 Organization-specific know how (12:39, 5 September 2020)
- 1.5.3.6 Documentation requirement for sample and material (12:40, 5 September 2020)
- 1.5.3.7 Retained personnel records (12:41, 5 September 2020)
- 1.5.4.1 Independence of internal compliance assessment (12:41, 5 September 2020)
- 1.5.4.2 Internal assessment of the organizations' quality professionals (12:42, 5 September 2020)
- ARRIVE Essential - Study design (16:24, 5 September 2020)
- ARRIVE Essential - Sample size (16:25, 5 September 2020)
- ARRIVE Essential - Inclusion and exclusion criteria (16:30, 5 September 2020)
- ARRIVE Essential - Randomization (16:33, 5 September 2020)
- ARRIVE Essential - Blinding (16:37, 5 September 2020)
- ARRIVE Essential - Statistical methods (16:39, 5 September 2020)
- ARRIVE Essential - Experimental animals (16:41, 5 September 2020)
- ARRIVE Essential - Experimental procedures (16:43, 5 September 2020)
- ARRIVE Essential - Results (16:45, 5 September 2020)
- 2.2.2 Use of template for (manual) data recording (17:18, 5 September 2020)
- 3.1.1 Platform to record data (17:34, 5 September 2020)