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
April 07-08, 2025
4th International Conference and Expo on Pharmaceutics & Novel Drug Delivery Systems
Vancouver, Canada
May 16-17, 2025
8th International Conference on Pharmaceutical Research
&
Innovations in Pharma Industry
Rome, Italy
June 02-03, 2025
31st International Conference on Advanced Clinical Research and Clinical Trials
Amsterdam, Netherlands
June 10-11, 2025
24th International Conference on Medicinal and Pharmaceutical Chemistry
Vancouver, Canada
June 10-11, 2025
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June 23-24, 2025
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Paris, France
July 21-22, 2025
11th International Conference on Antimicrobials & Antibiotic Resistance
Vancouver, Canada
August 25-26, 2025
11th International Conference on Pharmaceutical Regulatory Affairs and IPR
Vancouver, Canada
September 08-09, 2025
13th International Conference and Exhibition on Natural Products and Medicinal Plants Research
Frankfurt, Germany
September 08-09, 2025
26th International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems
Frankfurt, Germany
September 15-16, 2025
42nd International Conference on Drug Discovery and Drug delivery system
Paris, France
September 22-23, 2025
20th International Conference on Pharmaceutical Formulations & Drug Delivery
Toronto, Canada
September 23-24, 2025
10th International Conference on Future Pharma and Innovations
Amsterdam, Netherlands
November 13-14, 2025
28th International Conference and Exhibition on Pharmaceutical Formulations
Aix-en-Provence, France
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
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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- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Next Generation Approach of Antibiotics - Antibiotics Resistance 2025 (Canada)
- Toxicology - Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
- Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
- Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)