Design Verification Done Right: Smarter Strategies For Prefillable Syringes

Design verification for prefillable syringes is becoming increasingly complex as development teams navigate evolving regulatory expectations, drug-device integration challenges, and limited practical guidance for establishing a robust, defensible testing strategy. This webinar provides a structured, risk-based approach to bringing greater clarity and consistency to the design verification process.

Using a real-world case study, the session will present a practical best-practice framework for planning, executing, and justifying design verification programs for prefillable syringes. Viewers will learn how to translate intended use, user requirements, Quality Target Product Profile (QTPP) elements, and Essential Drug Delivery Outputs into a fit-for-purpose verification strategy — including test selection, acceptance criteria, sample-size rationale, and aging considerations.

Designed for teams working on combination products, injectable drug delivery systems, and prefilled syringe development, this presentation also provides actionable insights to help reduce ambiguity, strengthen development decisions, and establish a more consistent and defensible approach to verification planning.