November 25, 2024
Webinars Prefilled Apiject Injector

Transitioning your Drug Product or Vaccine into a Prefilled BFS Delivery Device

• Develop an understanding of the technical factors involved in transitioning your drug product, including material compatibility, process parameters, and their effects on drug stability and integrity.

• Identify and resolve potential issues by utilizing prototyping and feasibility studies to ensure the BFS system meets necessary performance and quality standards.

• Considerations when assessing drug or vaccine formulation, packaging, regulatory filings, and biowaiver requests for combination product development via BFS technology.