Difference between revisions of "1.5.2.4 Principal investigators and study directors"
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== A. Background & Definitions == | == A. Background & Definitions == | ||
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== B. Guidance & Expectations == | == B. Guidance & Expectations == | ||
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* Enforces a climate of good scientific practice, rigor and reproducibility, and continued excellence in preclinical data. | * Enforces a climate of good scientific practice, rigor and reproducibility, and continued excellence in preclinical data. | ||
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* Establishes effective communication with research team and quality professionals (if present); enables training for research team so that approriate expertise is guaranteed to conduct with the appropriate quality needs. | * Establishes effective communication with research team and quality professionals (if present); enables training for research team so that approriate expertise is guaranteed to conduct with the appropriate quality needs. | ||
| − | + | * Develops the [[2.1.1 Study protocol]] and ensures all procedures specified in the study protocol including amendments are followed and all data generated during a study are fully traceable and documented. Makes study protocol and amendments available to research team and quality professionals. | |
| − | * Develops the [[Study | + | * Ensure that all raw data generated are fully documented and recorded; Signs and dates the final report to indicate acceptance of responsibility for the validity of the data; Ensures that, after completion of the study, the study protocol, the final report, raw data and supporting material are archived. |
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| − | * Ensure that all raw data generated are fully documented and recorded; Signs and dates the final report to indicate acceptance of responsibility for the validity of the data; Ensures that, after completion of the study, the study | ||
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== C. Resources == | == C. Resources == | ||
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Latest revision as of 12:54, 24 March 2021
A. Background & Definitions
to be added
B. Guidance & Expectations
* Enforces a climate of good scientific practice, rigor and reproducibility, and continued excellence in preclinical data.
- Establishes effective communication with research team and quality professionals (if present); enables training for research team so that approriate expertise is guaranteed to conduct with the appropriate quality needs.
- Develops the 2.1.1 Study protocol and ensures all procedures specified in the study protocol including amendments are followed and all data generated during a study are fully traceable and documented. Makes study protocol and amendments available to research team and quality professionals.
- Ensure that all raw data generated are fully documented and recorded; Signs and dates the final report to indicate acceptance of responsibility for the validity of the data; Ensures that, after completion of the study, the study protocol, the final report, raw data and supporting material are archived.
C. Resources
to be added
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