Full Event Guide


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Take a look at what you can gain across 3-days including:

  • 3 in-depth workshops covering
      • How to increase injectable device connectivity while mitigating risks
      • Integration of Essential Performance Requirements of your injectable device development for submission and approval (led by Laurie Auerbach, Principal Consultants, Compliance Prodigies LLC)
      • Putting human factors into context and extending applications for home-use injectable device (led by Sanofi and Gilead)
  • 16+ insightful case studies across high volume, high viscosity subcutaneous device engineering, next gen onbody device development and tackling EU MDR from Regeneron, Takeda, Alnylam, Biomarin
  • Learn advanced CCIT testing to ensure robustness and quality of your injectable device products from Datwyler and Gilead