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June 28-30, 2016

Palm Springs, California

Full Event Guide

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This year’s agenda has been refined by our expert scientific advisory board to provide you with a detailed end to end inspection of the drug-device development process.

• Analyze the Impact of Extractables and Leachables

• Integrate Quality Control Systems

• Consolidate International Regulatory Approval

Download the full event guide here.


For an insight into last year’s PFS-Tech summit meeting, download your free presentation pack here.

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Past Presentations Pack

Including:

  • Suzzette Roan, Associate Director Regulatory Affairs CMC, Combination Products & Medical Devices, Biogen
  • Diane Doughty, Scientist, Drug Delivery & Devices, MedImmune
  • Wendy Shieu, Engineer II, Genentech
  • Stephen Barat, Executive Director, Non-Clinical and Translational Sciences Safety Assessment and Bioanalysis, Actavis
  • Tiffany McIntire, Human Factors Engineer, Eli Lilly