Clinical Trial Auditing
To determine whether the actions related to the establishment and monitoring of this clinical research were performed successfully, if the data were gathered, evaluated, and reported in line with the protocol, standard operating procedures were reviewed independently and methodically. System audits should be manageable with the available resources and of a size that is reasonable (can be managed). Audits must be planned and carried out in order to produce outcomes that are deemed acceptable. Most critical, leave windows open for unplanned audits and don't reduce your audit programme.
- Pre-study Qualification Visit
- Monitoring of Clinical Trials
- Auditing of Clinical Trials
Related Conference of Clinical Trial Auditing
February 27-28, 2025
8th International on Pharmacy and Pharmaceutical Conference
Prague, Czech Republic
April 07-08, 2025
4th International Conference and Expo on Pharmaceutics & Novel Drug Delivery Systems
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31st International Conference on Advanced Clinical Research and Clinical Trials
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10th International Conference on Future Pharma and Innovations
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Clinical Trial Auditing Conference Speakers
Recommended Sessions
- Adaptive Trial Model
- Artificial Intelligence in Clinical Trials
- Clinical and Medical Case Reports
- Clinical Data Management
- Clinical Data Strategy and Analytics
- Clinical Research Using Bioinformatics
- Clinical Trails and Innovation
- Clinical Trial Auditing
- Clinical Trials in Cardiology and Neurology
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