PFS East Coast - Device Usability & mRNA PFS Scale Up

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Hi there,

As the injectable drug devices landscape continues to expand, the industry is navigating key developments in device usability, evolving patient expectations, and the PFS scale‑up required to support complex modalities such as mRNA. Day Two of the PFS & Injectable Drug Devices East Coast conference brings these areas into focus.

Sessions highlights include:

Rethinking Device Substitutability: Human Factors Innovation for Generics & Biosimilars

Mark DeStefano, Global Technology Innovation, Combination Products and Device Research & Development, Teva Pharmaceuticals

Navigating the Complexities of mRNA PFS Scale-up: Development, Timelines and Supply

Christina Van Geen Hoven, Director and Portfolio Project Lead, Pfizer

Closing the Loop: Smarter Complaint Handling for Auto-Injector Combination Products

Edward Hatton, Director Quality Assurance, External Manufacturing, Amneal Pharmaceuticals

Plus - Global Perspectives on Subcutaneous Injection: Patient Needs and Barriers Across Three Markets, with Adrienne Fletcher, Director, Packaging and Device Strategy and Innovation, Johnson & Johnson, and Johanna Schoss, Principal Human Factors Engineer, Biogen.

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Interested in attending?

Vendor companies register here.

Big Pharma and Biotech companies, please join us as a
complimentary guest. Go here to register*.

*Terms and conditions apply

We look forward to welcoming you in Boston in April 2026.

Best regards,

The SAE Pharma Team

Michael Fraser
Head of Strategic Partnerships
Get in touch today
T: +44 (0) 20 7827 6018

Abigail Owen
Business Development Executive
Get in touch today
T: +44 (0) 20 7827 6725