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Final Chance to Save! Register by February 3 and Save up to $200!


The manufacturing environment within our industry is changing rapidly in response to new products with increasing complexity, evolving regulatory expectations, changing technologies, and a need to improve our manufacturing performance.


Gain the newest and most comprehensive information about traditional and biopharmaceutical science, manufacturing technology, quality and evolving regulations from leading subject matter experts at PDA’s premier event, the 2015 PDA Annual Meeting. Leading the discussions:


• Jeff Boyd, Head of Technical Operations & Gene Therapies Unit, Novartis


• Michael O’Brien, Head, Pharmaceutical Sciences, Pfizer Inc.


• Jeff Levy, Vice President, Technical Services, Manufacturing Science,


Eli Lilly & Company


The 2015 PDA Annual Meeting is the only event that gives you a view into the future, enabling you and your company to prepare today for the industry of tomorrow.


Want to learn more? From March 19-20, five in-depth education courses will be held. These courses will teach you about:


• Technical and Regulatory Challenges of Combination Drug Delivery


Products – Pre-filled Syringes, Autoinjectors and Injection Pens (March 19)


• NEW COURSE The Quality Culture and Its Measurement (March 19)


• NEW COURSE Applying Six Sigma Techniques to the Process Validation


Lifecycle (March 19)


For more information and to register, please visit pdaannualmeeting.org Join the conversation at #PDAAnnual


The Parenteral Drug Association presents... 2015 PDA Annual Meeting


March 16-18, 2015 Red Rock Casino Resort and Spa, Las Vegas, NV


Exhibition: March 16-17 Post-Conference Workshop: March 18-19 Courses: March 19-20


Manufacturing Innovation and Efficiency: Achieving Quality Performance in Sterile and Biopharmaceutical Operations


• Sterile Pharmaceutical Dosage Forms: Basic Principles (March 19-20)


• Developing a Robust Supplier Management Process (March 20)


• Thomas Pizzuto, Vice President, Johnson and Johnson


• Mark McCamish, Global Head, Biopharmaceutical Development,


Sandoz International GmbH


• Sumant Ramachandra, MD, PhD, MBA, Senior Vice President R&D,


Medical and Regulatory Affairs, Chief Scientific Officer, Hospira


• And many more!


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