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- 3.1.2.1 Traceability of data and any person having impact on data
- 3.1.2.1 Traceability of data and any person having impact on data
- 3.1.2.2 Process for witnessing of records
- 3.1.2 Procedures for how and when to record data
- 3.1.3 Data security
- 3.2.1 General guidance on training
- 3.2.2 Good Research Practice training
- 3.2.3 Implementation of the EQIPD Quality System
- 3.2.4 Training on specific methods, tasks and activities
- 3.3.1 Fit-for-purpose working environment
- 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use
- 3.3.3 Management of research materials and reagents
- 3.4.1.10 Surgical procedures
- 3.4.1.11 Animal euthanasia procedures
- 3.4.1.1 Ethical evaluation and authorization process of animal use
- 3.4.1.2 Animal procurement & identification
- 3.4.1.3 Animal housing conditions
- 3.4.1.4 Animal environmental conditions
- 3.4.1.5 Food, watering and bedding
- 3.4.1.6 Sanitation procedure
- 3.4.1.7 Frequency and procedure of observation of animals
- 3.4.1.8 Animal health and genetic monitoring
- 3.4.1.9 Veterinary interventions during the study
- 3.4.1 Animal characteristics, care and use
- 3.4.2.1 Cell culturing
- 3.4.2.2 Antibody validation
- 3.4.2.3 Biological and technical replicates
- 3.5.1 Animal and non-animal method and assay qualification
- 3.5.2 Protocols for methods and assays
- 3.5.3 Minimum reporting guidelines
- 3 Support Processes
- 4.1.1 Risk assessment
- 4.1.2 Self assessment
- 4.1.3 External Assessment
- 4.1.3 External assessment
- 4.2.1 Installation of solutions, actions and mitigation strategies
- 4.2.2 Error and incident management
- 4.2.3 Responsible conduct of research
- 4.2.4 Key performance indicators
- 4.3.1.1 Adding new items
- 4.3.1.2 Deleting items
- 4.3.1.3 Revising items
- 4.3.2.1 Using the Planning Tool
- 4.3.2.2 Creating NEEDs
- 4.3.2.3 Revising NEEDs
- 4.3.2.4 Deleting NEEDs
- 4.3.2 Using the EQIPD applications
- 4 Continuous improvement
- ARRIVE 2.0
- ARRIVE Essential - Blinding