Ready-to-use components eliminate the need for component preparation by the drug product manufacturer, enabling them to streamline their processes and focus on their core competencies, such as drug product development and manufacturing.
Drug product and parenteral packaging component manufacturers are continuously evolving in alignment with the advancements in technology and increasing regulatory requirements to better ensure the quality and safety of injectable drug products for patients. The incorporation of barrier technology and flexible fillers and the use of ready-to-use (RTU) packaging components are rapidly gaining adoption as safe and effective solutions for fill/finish processes and container closure systems, respectively.
Read this article from Pharmaceutical Technology’s Biologics and Sterile Drug Manufacturing 2018 eBook.
Pharmaceutical Technology
eBook: Biologics and Sterile Drug Manufacturing
Vol. 42
May 2018
Pages: 44–46
When referring to this article, please cite it as S. Cote, “Ready-to-Use Parenteral Packaging Components Address Evolving Aseptic Fill/Finish Requirements,” Pharmaceutical Technology Biologics and Sterile Drug Manufacturing eBook (May 2018).
Drug Solutions Podcast: A Closer Look at mRNA in Oncology and Vaccines
April 30th 2024In this episode fo the Drug Solutions Podcast, etherna’s vice-president of Technology and Innovation, Stefaan De Koker, discusses the merits and challenges of using mRNA as the foundation for therapeutics in oncology as well as for vaccines.
Understanding the Variability in Bioburden Test Results in Biomanufacturing
May 7th 2025This article explores the impact of test volume, microbial distribution, and dilution errors on bioburden testing variability. It presents statistical approaches to estimate percentage error and discusses strategies to optimize microbial enumeration techniques in biopharmaceutical quality control.