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
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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
- Clinical Trials in Dermatology and Oncology
- Clinical Trials in the Future
- Drug Safety and Pharmacovigilance
- Imaging Research
- Oncology Clinical Research
- Patient-Centric Clinical Trials
- Post Marketing Surveillance
- Research and Clinical Trials Ethics
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