Difference between revisions of "Core Requirements"

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|'''Core Requirement'''
 
|'''Core Requirement'''
 
|​'''Toolbox reference'''
 
|​'''Toolbox reference'''
−
|​'''Documents required'''
+
|​'''EQIPD provided templates<sup>*</sup>'''
 
|-
 
|-
 
|rowspan="2"|'''Research team'''​
 
|rowspan="2"|'''Research team'''​
 
|1
 
|1
−
|Process owner must be identified for the Quality System
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|Process owner for the Quality System must be identified
 
|[[1.5.2.3 Process owner]]​
 
|[[1.5.2.3 Process owner]]​
−
|No specific document needed
+
| -
 
|-
 
|-
 
|2
 
|2
 
|Communication process must be in place
 
|Communication process must be in place
 
|[[1.2 Scope]]
 
|[[1.2 Scope]]
−
|Template
+
|[https://paasp.sharepoint.com/:w:/s/EQIPD/ERyfFP_pBytDiEfqCutDAJQBFbaGQEx3G1pyOmDl50o_LQ?e=wlkvHJ Communication plan]
 
|-
 
|-
 
|rowspan="3"|'''Quality culture'''
 
|rowspan="3"|'''Quality culture'''
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|The research unit must have defined quality objectives ​
 
|The research unit must have defined quality objectives ​
 
|[[1.1 Mission]]
 
|[[1.1 Mission]]
−
|Template
+
|[https://paasp.sharepoint.com/:w:/s/EQIPD/EVUTrgQRuNpKtpHkobdCOq4BhSTw1p3akXGKvI_MRgxYag?e=dJoZ5T Mission statement]
 
|-
 
|-
 
|4
 
|4
 
|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)]
 
|-
 
|-
 
|5
 
|5
 
|The research unit must have a procedure to act upon concerns of potential misconduct
 
|The research unit must have a procedure to act upon concerns of potential misconduct
 
|[[4.2.3 Responsible conduct of research]]
 
|[[4.2.3 Responsible conduct of research]]
 +
| -
 
|-
 
|-
 
|rowspan="4"|​​'''Data integrity'''
 
|rowspan="4"|​​'''Data integrity'''
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|Generation, handling and changes to data records must be documented
 
|Generation, handling and changes to data records must be documented
 
|​[[2.3.1 Generation, recording, handling and archiving of raw data]]
 
|​[[2.3.1 Generation, recording, handling and archiving of raw data]]
−
|Template
+
|rowspan="3"|[https://paasp.sharepoint.com/:w:/s/EQIPD/EQTANrsKHTVIqtO8LT-ZJIEBEUJVZI6siRLkHfliUD4gdA?e=GJusMa Documentation plan]
 
|-
 
|-
 
|7
 
|7
 
|Data storage must be secured at least for as long as required by legal, contractual or other obligations or business needs
 
|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]]​
 
|[[3.1.3 Data security]]​
−
|Template
 
 
|-
 
|-
 
|8
 
|8
 
|Reported research outcomes must be traceable to experimental data
 
|Reported research outcomes must be traceable to experimental data
 
|[[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​]]
−
|Template
 
 
|-
 
|-
 
|9
 
|9
 
|Reported data must disclose all repetitions of a study, an experiment, or a test regardless of the outcome​​
 
|Reported data must disclose all repetitions of a study, an experiment, or a test regardless of the outcome​​
 
|[[2.4 Reporting]]
 
|[[2.4 Reporting]]
−
|No specific document needed
+
| -
 
|-
 
|-
 
|rowspan="5"|​​​'''Research processes'''
 
|rowspan="5"|​​​'''Research processes'''
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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]]
−
|No specific document needed, but document in Study plan
+
|[https://paasp.sharepoint.com/:w:/s/EQIPD/EbuGPqIAiTtKlmRQJ7bSy_0BfmYNqXl-W6Reh3tW5vAIzQ?e=ycqEuG Study protocol]
 
|-
 
|-
 
|11
 
|11
 
|All personnel involved in research must have adequate training and competence to perform assigned tasks
 
|All personnel involved in research must have adequate training and competence to perform assigned tasks
 
|[[3.2.1 General guidance on training]]
 
|[[3.2.1 General guidance on training]]
−
|No specific document needed
+
| -
 
|-
 
|-
 
|12
 
|12
 
|Protocols for experimental methods must be available
 
|Protocols for experimental methods must be available
 
|[[3.5.2 Protocols for methods and assays]]
 
|[[3.5.2 Protocols for methods and assays]]
−
|No specific document needed except the protocols
+
|[https://paasp.sharepoint.com/:w:/s/EQIPD/EfUO3B7RFxdHgxQ8JY5hhFoBEDUiPGK4C8n6BBHEprwroA?e=8IezWV Protocols for experimental methods]
 
|-
 
|-
 
|13
 
|13
 
|Adequate handling and storage of samples and materials must be ensured
 
|Adequate handling and storage of samples and materials must be ensured
 
|[[3.3.3 Management of research materials and reagents]]
 
|[[3.3.3 Management of research materials and reagents]]
−
|No specific document needed
+
| -
 
|-
 
|-
 
|14
 
|14
 
|Research equipment and tools must be suitable for intended use and ensure data integrity
 
|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]]
 
|[[3.3.2 Processes to enable computerized and non-computerized systems being suitable for intended use]]
−
|No specific document needed
+
| -
 
|-
 
|-
 
|rowspan="3"|'''Continuous performance'''
 
|rowspan="3"|'''Continuous performance'''
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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]]​​
−
|To be documented with experimental protocol or a risk assessment protocol if performed
+
|[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]
 
|-
 
|-
 
|16
 
|16
 
|Critical incidents and errors during study conduct must be analyzed and appropriately managed
 
|Critical incidents and errors during study conduct must be analyzed and appropriately managed
 
|[[4.2.2 Error and incident management]]
 
|[[4.2.2 Error and incident management]]
−
|No specific document needed, but errors should be documented with the experimental protocol
+
|[https://paasp.sharepoint.com/:w:/s/EQIPD/EatOAFgLbctEvxRZTuSCdU4Bv8J1I_BitfKl-JJiieOTLA?e=z99RR1 Error reporting template]
 
|-
 
|-
 
|17
 
|17
 
|An approach must be in place to monitor the performance of the EQIPD Quality System, and address identified issues​
 
|An approach must be in place to monitor the performance of the EQIPD Quality System, and address identified issues​
 
|[[4.1.2 Self assessment]]
 
|[[4.1.2 Self assessment]]
−
|Template Self assessment available
+
|[https://paasp.sharepoint.com/:x:/s/EQIPD/EXjMqJ74JcpLh9x8_UN7EmkBzgAcgODVOTKlDWnAPnIpvw?e=PWwGJY Self assessment]
 
|-
 
|-
 
|'''Sustainability'''
 
|'''Sustainability'''
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|Resources for sustaining the EQIPD Quality System must be available
 
|Resources for sustaining the EQIPD Quality System must be available
 
|[[1.5.5 Sustainability]]
 
|[[1.5.5 Sustainability]]
−
|No specific document needed
+
| -
 
|}
 
|}
 +
<sup>*</sup>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]]​.​​​​
 
Back to the [[EQIPD Quality System]]​.​​​​

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​.​​​​

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