ACI s inaugural conference on
Clinical Supply Chain Optimization 2011 will equip clinical trial and supply professionals with the continuing knowledge, preparation, supply optimization tools and insight into leading edge technologies for effectively executing successful future overseas projects.
This conference will provide a series of novel and unique solutions to your organization s clinical supply challenges and help you reduce time-to-market on future drug products through successful trial execution. It has never been more crucial to the success of your organization to discover new clinical supply chain tools, technologies and best practices to stay ahead of the game and remove unnecessary waste and cost.
Key topics to be discussed include:
- Learn to build a Project Management Core Competency Team within your clinical supply chain from Merck & Co., Inc., Takeda and Biogen Idec
- Meeting and complying with USDA APHIS Requirements for importing clinical trial materialsfrom Anika Therapeutics, Merck & Co. and the U.S. FDA.
- Completing and successfully managing Emerging Market and Overseas Clinical Trials with real-life case studies from Pfizer, Human Genome Sciences and Cerexa Pharmaceuticals
- Examining the benefits of using IVRS to Enhance your Clinical Supply Management from Daiichi Sankyo and Vertex Pharmaceuticals
- Developing and improving your Trial Relationship with your CRO to enhance supply with key tools and best practices from Novartis, Otsuka Pharmaceutical and Medtronic Vascular
- Discovering key techniques and proven strategies to Minimizing Drug Supply Issues during a global clinical trial with Genzyme and Sepracor
Benefit from focused industry presentations and discussions from leading global clinical supply chain experts including
Merck & co, Pfizer, Inc, GlaxoSmithKline, Sepracor, Genzyme, Novartis, Daiichi Sankyo, Takeda, Allergan, Human Genome Sciences, Otsuka Pharmaceutical, Vertex Pharmaceuticals and many more multiple-sized drug development organizations. Additionally, hear directly from the
FDA and
TSA regarding regulatory compliance and fundamental importing/exporting opportunities for your supply distribution.
Additionally, do not miss the focused pre-conference workshops on
Overcoming the challenges of managing successful global trials and
Quality and efficiency for cost and temperature controlled transportation of your clinical supplies .Don t miss this unique opportunity to network with leading pharmaceutical, biotech and clinical research organizations who have implemented tools and strategies in order to cut cycle time and cost from their trials while managing trial risk effectively.
Register now by calling
888-224-2480, faxing your registration form to
877-927-1563 
