June 28-30, 2016

Palm Springs, California

Full Event Guide

Brochure thumbnail

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.

PFS-Tech Presentation Pack Thumb

Past Presentations Pack


  • 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