Clinical Supply Management
The value of some study drugs can reach tens of millions of dollars, making it essential to avoid overproduction, oversupply, and inventory expiration. With the high costs and strict handling requirements for many biopharmaceutical products entering clinical development, the logistics of clinical trial supplies are more critical than ever. Expert management begins with the clinical trial supply strategy, and ends with returns and destruction. Integration and coordination of many third-party vendors and technical systems is needed to verify that study drugs are available in sufficient quantity and quality at the various stages of clinical distribution. Clinical supplies management provides full traceability of drug supply from manufacturing to dispensation and destruction - making it a key factor in study success, as it avoids information gaps and reduces risks such as out of stock or expiration.
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Clinical Supply Management Conference Speakers
Recommended Sessions
- Bioethics and Regulatory Compliance
- Clinical Data Management and Analytics
- Clinical Operations & Project Management
- Clinical Research & Clinical Trials: Academic Perspective
- Clinical Supply Management
- Clinical Trial Forecasting, Budgeting and Contracting
- Clinical Trial Site Selection and Management
- Clinical Trials on different Diseases
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- Drug Discovery and Development
- Enrollment Planning and Patient Recruitment
- Future of Clinical Trials and Technology Innovations
- Globalization of Clinical Trials
- Innovations in clinical study designs
- Medical and Clinical Case Reports
- Medical Imaging in Clinical Research
- Patient-Centric Clinical Trials
- Pharmaceutical Sciences
- Pharmacovigilance and Drug Safety
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