Pages with the fewest revisions
Showing below up to 100 results in range #1 to #100.
View (previous 100 | next 100) (20 | 50 | 100 | 250 | 500)
- ARRIVE Essential - Experimental procedures (1 revision)
- 1.4.2.3 Radioactivity (1 revision)
- 1.4.2.5 Risks to unborn life (1 revision)
- ARRIVE Essential - Randomization (1 revision)
- ARRIVE Essential - Results (1 revision)
- ARRIVE Essential - Sample size (1 revision)
- 4.3.1.3 Revising items (1 revision)
- Hauptseite (1 revision)
- 2.1.1 Study (experimental) plan (1 revision - redirect page)
- Implementation Strategy (1 revision - redirect page)
- 1.4.3.1 Quality in collaborative research (1 revision - redirect page)
- 2.4.1 Non-public reporting (1 revision)
- Challenges (1 revision)
- Internal assessment (1 revision)
- 4.3.2.4 Deleting NEEDs (1 revision)
- 4 Continuous improvement (1 revision)
- 1.4.2.1 Biosafety (1 revision)
- 1.5.3 Management of resources (2 revisions)
- Why quality matters (2 revisions)
- 1.5.2.1 Organigram (2 revisions)
- 1.5.4.1 Independence of internal compliance assessment (2 revisions)
- 3.4.1.7 Frequency and procedure of observation of animals (2 revisions)
- 1.4.2.4 Genetically modified organisms (2 revisions)
- 1.5.2.2 Management (2 revisions)
- 1.5.4.2 Internal assessment of the organizations' quality professionals (2 revisions)
- 3.2.1 General guidance on training (2 revisions)
- 3.4.1.8 Animal health and genetic monitoring (2 revisions)
- 3.4.1.9 Veterinary interventions during the study (2 revisions)
- 4.2.4 Key performance indicators (2 revisions)
- 1.4.2.6 Handling of controlled substances (2 revisions)
- 4.3.1.1 Adding new items (2 revisions)
- 1.4.2.8 Human data protection (2 revisions)
- 1.5.2.6 Supporting team (2 revisions)
- 3.3.1 Fit-for-purpose working environment (2 revisions)
- 3.4.2.2 Antibody validation (2 revisions)
- ARRIVE Essential - Statistical methods (2 revisions)
- 1.3.2 Sources of pressure and bias-producing communication of pressure (2 revisions)
- 3.5.1 Animal and non-animal method and assay qualification (2 revisions)
- Abbreviations (2 revisions)
- 1.5.3.1 Personnel (2 revisions)
- 1.5.3.2 Facilities (2 revisions)
- 3.4.1.11 Animal euthanasia procedures (2 revisions)
- 1.5.3.3 Laboratory and experimental equipment used for measurement (2 revisions)
- 1.5.3.4 Electronic information system (2 revisions)
- 1.5.3.5 Organization-specific know how (2 revisions)
- 1.5.3.6 Documentation requirement for sample and material (2 revisions)
- 4.1.3 External Assessment (2 revisions)
- ARRIVE Essential - Blinding (2 revisions)
- 1.5.3.7 Retained personnel records (2 revisions)
- ARRIVE Essential - Experimental animals (2 revisions)
- 1.4.2.2 Chemical safety (3 revisions)
- 4.2.1 Installation of solutions, actions and mitigation strategies (3 revisions)
- ARRIVE Essential - Inclusion and exclusion criteria (3 revisions)
- 2.2.2 Use of template for (manual) data recording (3 revisions)
- 3.4.2.1 Cell culturing (3 revisions)
- 1.3.1 Transparency (3 revisions)
- ARRIVE Essential - Study design (3 revisions)
- Information on the calculation of the priority ranking (3 revisions)
- 1.3.3 Promotion criteria within a research unit (3 revisions)
- 3.4.1.10 Surgical procedures (3 revisions)
- 1.3.4 Performance criteria and assessment (3 revisions)
- 2.4.2 Publication (3 revisions)
- 3.4.1.2 Animal procurement & identification (3 revisions)
- Dossier (3 revisions)
- 1.4.3.4 Academia-academia: Research as collaboration (3 revisions)
- 3.4.1.3 Animal housing conditions (3 revisions)
- 3.4.1.4 Animal environmental conditions (3 revisions)
- 3.4.1.5 Food, watering and bedding (3 revisions)
- 3.4.1.6 Sanitation procedure (4 revisions)
- ARRIVE Essential - Outcome measures (4 revisions)
- 3.2.2 Good Research Practice training (4 revisions)
- 1.5.2.4 Principal investigators and study directors (4 revisions)
- 2.3.1.1 Converting non-electronic information into an electronic form (4 revisions)
- 1.4.2.7 Animal care and use (4 revisions)
- 1.5.2.7 Quality professionals (4 revisions)
- 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use (4 revisions)
- 3.4.2.3 Biological and technical replicates (4 revisions)
- 1.5.2 Roles and responsibilities of involved personnel and organization (4 revisions)
- 2.3.4 Data visualization (4 revisions)
- 3.3.3 Management of research materials and reagents (4 revisions)
- 3.5.3 Minimum reporting guidelines (4 revisions)
- 2.4 Reporting (4 revisions)
- 3.4.1.1 Ethical evaluation and authorization process of animal use (4 revisions)
- 3 Support Processes (4 revisions)
- 2.1.5 Pre-specification (4 revisions)
- Risk Management Case Studies (4 revisions)
- 1.4.1 Research ethics (4 revisions)
- 3.1.2.2 Process for witnessing of records (4 revisions)
- 2.2.1 Use of SOPs for standard experiments (5 revisions)
- 3.1.3 Data security (5 revisions)
- 3.1.2.2 Process for witnessing of records (5 revisions)
- 1.5.2.3 Process owner (5 revisions)
- Experimental Record (5 revisions)
- 1.5.5 Sustainability (5 revisions)
- 1.5.2.5 Research team (5 revisions)
- 2.1.10 Plausibility check (5 revisions)
- 3.2.4 Training on specific methods, tasks and activities (5 revisions)
- 4.3.1.2 Deleting items (5 revisions)
- 2.1.2 Unique study ID (5 revisions)
- 3.1.2.1 Traceability of data and any person having impact on data (5 revisions)