Difference between revisions of "Core Requirements"
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|rowspan="2"|'''Research team''' | |rowspan="2"|'''Research team''' | ||
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| − | |Process owner | + | |Process owner for the Quality System must be identified |
|[[1.5.2.3 Process owner]] | |[[1.5.2.3 Process owner]] | ||
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|All activities must comply with relevant legislation and policies | |All activities must comply with relevant legislation and policies | ||
|[[1.4.2 Adherence to legal and regulatory considerations]] | |[[1.4.2 Adherence to legal and regulatory considerations]] | ||
| − | | | + | |[https://paasp.sharepoint.com/:w:/s/EQIPD/ET18tqgUVfJCsYNYxexlgA8BnwRLEn0k8JcFmeQlTiQMoA?e=zoXuUf Checklist for preparing an animal care and use program description (for organizations without accreditation by AAALAC or equivalent)] |
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|5 | |5 | ||
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|Investigator must declare in advance whether a study is intended to inform a formal knowledge claim | |Investigator must declare in advance whether a study is intended to inform a formal knowledge claim | ||
|[[2.1.4 Purpose of research]] | |[[2.1.4 Purpose of research]] | ||
| − | |[https://paasp.sharepoint.com/:w:/s/EQIPD/ | + | |[https://paasp.sharepoint.com/:w:/s/EQIPD/EbuGPqIAiTtKlmRQJ7bSy_0BfmYNqXl-W6Reh3tW5vAIzQ?e=ycqEuG Study protocol] |
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|Risk assessment must be performed to identify factors affecting the generation, processing and reporting of research data | |Risk assessment must be performed to identify factors affecting the generation, processing and reporting of research data | ||
|[[4.1.1 Risk assessment]] | |[[4.1.1 Risk assessment]] | ||
| − | |[https://paasp.sharepoint.com/:w:/s/EQIPD/ | + | |[https://paasp.sharepoint.com/:w:/s/EQIPD/EbuGPqIAiTtKlmRQJ7bSy_0BfmYNqXl-W6Reh3tW5vAIzQ?e=ycqEuG Study protocol] and [https://paasp.sharepoint.com/:x:/s/EQIPD/ETo9OwIvZpNHtepp6IvxylQBjtjhk2AmRnypLCIOrGwMvA?e=n1zy3X Risk assessment template] |
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Latest revision as of 17:55, 10 May 2021
| Categories | No | Core Requirement | Toolbox reference | EQIPD provided templates* |
| Research team | 1 | Process owner for the Quality System must be identified | 1.5.2.3 Process owner | - |
| 2 | Communication process must be in place | 1.2 Scope | Communication plan | |
| Quality culture | 3 | The research unit must have defined quality objectives | 1.1 Mission | Mission statement |
| 4 | All activities must comply with relevant legislation and policies | 1.4.2 Adherence to legal and regulatory considerations | Checklist for preparing an animal care and use program description (for organizations without accreditation by AAALAC or equivalent) | |
| 5 | The research unit must have a procedure to act upon concerns of potential misconduct | 4.2.3 Responsible conduct of research | - | |
| Data integrity | 6 | Generation, handling and changes to data records must be documented | 2.3.1 Generation, recording, handling and archiving of raw data | Documentation plan |
| 7 | Data storage must be secured at least for as long as required by legal, contractual or other obligations or business needs | 3.1.3 Data security | ||
| 8 | Reported research outcomes must be traceable to experimental data | 3.1.2.1 Traceability of data and any person having impact on data | ||
| 9 | Reported data must disclose all repetitions of a study, an experiment, or a test regardless of the outcome | 2.4 Reporting | - | |
| Research processes | 10 | Investigator must declare in advance whether a study is intended to inform a formal knowledge claim | 2.1.4 Purpose of research | Study protocol |
| 11 | All personnel involved in research must have adequate training and competence to perform assigned tasks | 3.2.1 General guidance on training | - | |
| 12 | Protocols for experimental methods must be available | 3.5.2 Protocols for methods and assays | Protocols for experimental methods | |
| 13 | Adequate handling and storage of samples and materials must be ensured | 3.3.3 Management of research materials and reagents | - | |
| 14 | Research equipment and tools must be suitable for intended use and ensure data integrity | 3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use | - | |
| Continuous performance | 15 | Risk assessment must be performed to identify factors affecting the generation, processing and reporting of research data | 4.1.1 Risk assessment | Study protocol and Risk assessment template |
| 16 | Critical incidents and errors during study conduct must be analyzed and appropriately managed | 4.2.2 Error and incident management | Error reporting template | |
| 17 | An approach must be in place to monitor the performance of the EQIPD Quality System, and address identified issues | 4.1.2 Self assessment | Self assessment | |
| Sustainability | 18 | Resources for sustaining the EQIPD Quality System must be available | 1.5.5 Sustainability | - |
*The provided templates are suggestions which may be used. However, it is not mandatory to use the templates developed by EQIPD. It is up to the research unit to modify them, develop new or use existing documentation.
For information on required documentation within EQIPD please visit: Documentation in EQIPD
Back to the EQIPD Quality System.
