SMi is proud to present the 5th Annual Pre-Filled Syringes West Coast Conference in San Diego on 15th and 16th June 2020.

Following the success of the last event, the Pre-Filled Syringes West Coast conference is back to uncover the latest innovations in combination product development, device design, human factors engineering and drug product formulation to give a holistic overview of the industry and what we can expect for the future.

With the global market for prefilled syringes estimated to exceed $ by 2025, this year’s agenda will encompass key drivers and hot topics of the industry including; updates to regulatory guidance from industry experts and regulatory bodies, case studies on device design and complex formulation, life cycle and control strategies, and innovations in connectivity and digital health.

This two-day agenda offers you peer-to-peer networking with Global Product Managers, Senior PFS Engineers, Device Testing Managers, Heads of Late-Stage PFS Development and many more.

PLUS, two interactive post conference workshops:

Workshop A: Connected devices and digital health: How to navigate the US FDA usability engineering requirements
Hosted by Shannon Clark, Principal, UserWise, Inc.

Workshop B: Postmarket safety reporting: The current regulatory environment with a global impact
Hosted by Khaudeja Bano, Sr. Medical Director, Abbott Molecular

Featured speakers include:

• Brittney Pachucki, Device Engineer, AstraZeneca
• Darin Zehrung, Global Program Leader, Medical Devices and Health Technologies,
  PATH
• Jace Blackburn, Smart Device Engineer, Genentech
• James P. Wabby, Executive Director, Regulatory Affairs – Device/Combination Products, Allergan
• Jian Liu, Senior Scientist, Amgen
• Khaudeja Bano, Senior, Medical Director, Abbott Diagnostics
• Larry Atupem,  Sr Business Development Specialist, Zeon 
• Maggie Reiff, Manager, Device Engineering, Pfizer
• Mark DeStefano, Assoc. Dir. CPD Feasibility, New Technology and Prototyping Development, Teva Pharmaceuticals
• Natalie Abts, Head of Human Factors Engineering, Genentech
• Robert Ovadia, Engineer II, Genentech
• Sarah Mollo, Combination Product Policy Analyst, FDA
• Severine Duband, Global Category Manager, Nemera
• Shannon Clark, Principal, UserWise, Inc.
• Takuya Minezaki, Research Manager, Mitsubishi Gas Chemical Company, Inc.
• Tina Rees, Associate Director - Human Factors, Ferring Pharmaceuticals
• Tracy Hsu, Associate Director, Ionis Pharmaceuticals

Key Reasons to Attend:

• Engage in case study presentations from leading pharma and biotech companies on complex product formulation and optimising device design to aid delivery
• Discuss show to optimise current processes to align with global regulatory updates
• Delve into human factors engineering best practices
• Uncover how industry is incorporating connectivity and digital health to optimise the user experience

Who should attend:

• Drug-delivery developers
• Medical Device Engineers
• Primary Packaging material designers
• Secondary packagers
• Smart device developers
• Training device developers
• Device-safety solution providers
• Drug developers

Early bird deadlines:

• Register by 28th February to save $400
• Register by 31st March to save $200
• Register by 30th April to save $100
   

To register or for more information visit:   

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