With the high costs of development for a new drug, no company can afford to further increase costs through inefficiencies in their clinical trial supply chain. A key reason for high costs is due to clinical supply chain and forecasting failures domestically, as well as high patient recruitment costs/challenges.
As global clinical trials continue to increase within emerging overseas markets, there has never been a more important time for drug development organizations to effectively manage and optimize their clinical supply chains. The growth of external, complex trials brings a unique set of challenges. These include
complying with multiple stringent regulations, cost-effective/validated distribution, clinical product management, risk mitigation, cost effective trial execution, and drug supply management issues.
Addressing these hurdles is fundamental in reducing time-to-market on future drug prospects, whilst helping gaining the competitive edge in this competitive market.
ExL’s 6th Forecasting & Optimizing Clinical Supply will provide a platform for clinical supply chain professions to hear case study examples, share best practices and discuss strategies for gaining efficiencies through better clinical supply forecasting. Learn what techniques other companies are pursuing, compare ROIs on forecasting technologies and take-home applicable information to
streamline clinical trials and reduce costs.
This conference will provide participants with the tools and knowledge to effectively communicate and increase transparency to better forecast clinical supply demand, manage clinical supply in emerging markets, understand the regulatory guidelines and expectations, increase operational efficiencies, and
learn new emerging forecasting technologies for global clinical supply chain excellence. This is a must attend event for professionals involved in the clinical supply chain looking to advance their knowledge and learn new strategies, while interacting with other pharmaceuticals, medical device, and
biotechnology professionals.
Who Should Attend
This conference is specifically designed for pharmaceutical, biotech, CRO and academic professionals specializing in:
- Clinical Trial Supply / Clinical Supplies / Operations
- Clinical Trial Logistics / Planning / Distribution
- Drug Supply Management
- Clinical Manufacturing, Packaging and Labeling
- Quality Assurance / Quality Control
- Clinical Pharmacy
- IVRS / IWRS
- Investigational Supplies
- Logistics and Distribution
- Clinical Trial Sourcing and Procurement
- Regulatory Affairs
- Data Management & Statistics
- External Alliances
- Clinical Research
- Project Management
This conference is also of interest to:
- Clinical Services/Clinical Process Improvement Providers
- Clinical Technologies Companies
- Forecasting and Simulation Technologies
- Clinical Packaging and Logistics Companies
- Contract Research Organizations
- Manufacturing Solution Providers
