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Biologics are transforming the healthcare landscape, broadening treatment options, and improving patient outcomes. This webinar will discuss three key trends that are shaping the lifecycle planning for containment and delivery of these biologics drug products.

  • Shift in Route of Administration
  • Regulations including Annex 1 and MDR
  • Increasing competition and price pressure

Transitioning from a vial to a prefilled syringe (PFS) is a complex process, and it’s important to understand the impact that your drug packaging selection can have on the success of the lifecycle of the drug, in all packaging formats that you plan to bring to market.

Join us for this insightful webinar with West experts to discuss how collaboration with your packaging supplier early in the drug development process can help navigate increased complex regulatory requirements and reduce time in your packaging development work.

Christa Jansen-Otten, expert in technical product development at West Pharmaceutical Services

Christa Jansen-Otten

Director Technical Product Development

Christa is the Director of Technical Product Development at West Pharmaceutical Services, Inc. With more than 20 years of extensive experience in the pharmaceutical industry, she is a recognized authority in the field of prefillable systems and delivery technology. Christa holds a diploma in Biomedical Engineering from the University of Aachen. Her career began as a Quality Assurance Manager at one of the world’s leading pharmaceutical companies, where she specialized in sterile filling and packaging. She later expanded her expertise in the Customer Quality Assurance department of a top manufacturer of prefillable syringes. Since joining West Pharmaceutical Services in 2005, Christa has excelled in various roles within the Technical Customer Service, Marketing, and Product Management departments. Her in-depth knowledge and innovative approaches have significantly contributed to advancements in prefillable systems and delivery technology. Christa is a sought-after speaker at worldwide conferences, where she shares her insights and experiences, contributing to industry advancements
Page McAndrew, expert in scientific communications at West Pharmaceutical Services

Page McAndrew

Director of Scientific Communications

T. Page McAndrew is Director of Scientific Communications at West Pharmaceutical Services, Inc., leading a team responsible for developing and publishing technical content that enables most effective use of West components/systems. He has B.S. in Chemistry from King’s College (PA), a Ph.D. in Chemistry from the University of Pennsylvania, and has authored 9 U.S. patents and over 70 publications.