Packaging Digest is part of the Informa Markets Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 8860726.

Medical Packaging

Key Factors in Transitioning to Combination Products

Article-Key Factors in Transitioning to Combination Products

Image credit: Olena Poliakevych/ iStock via Getty Images IMG_2023-2-27-084943.jpg
Learn the steps in de-risking drug and device integration in this webinar sponsored by West Pharmaceutical Services.

Combination products are undergoing tremendous growth, driven by the rise in chronic disease indications, demand for self-administered therapies, minimally invasive procedures, and technology advancements. However when transitioning from a vial system to a needle-based combination product, there are many challenges in areas of government regulations, supply chain complexity, and patient outcomes. This webinar addresses these challenges, proper life cycle management, and the transition to a combination product.

  • The steps to de-risking drug and device integration
  • Strategies to de-risk the product development process and user testing
  • A greater understanding of data needed to support device reliability and robustness

Jen Riter, Senior Director, Business and Technical Operations for Services & Solutions
West Pharmaceutical Services, and Daniel Bantz Manager, Scientific Communications, Self-Injection Systems
West Pharmaceutical Services, will be the speakers. 

Get registered here for this transformative webinar. 

Hide comments
account-default-image

Comments

  • Allowed HTML tags: <em> <strong> <blockquote> <br> <p>

Plain text

  • No HTML tags allowed.
  • Web page addresses and e-mail addresses turn into links automatically.
  • Lines and paragraphs break automatically.
Publish