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Manufacturing Processes
CDMO in Biopharma: Opportunity or risk?
Both, CDMOs and CMOs, are offering major opportunities in biopharma for startups and emerging companies as well as for established players who are approaching the limits of their manufacturing facilities or are generally looking to outsource parts of or their entire commercial production.
Michael Mühlegger
June 16, 2025
Manufacturing Processes
Mission completed – and now? What to do with the RoSS® Shell after use
Once they have fulfilled their purpose to protect valuable biologics, the question for our RoSS containers arises: What now? This is why we summarized information on the recycling of our containers for single use bags in this article.
Claus Exenberger
June 9, 2025
Manufacturing Processes
Upstream intensification from lab to mAb manufacturing
Upstream intensification processes use high density cell banking to optimize monoclonal antibody production. How does HDCB advance cell expansion? And is seed train intensification relevant to biosimilars?
Brian Moloney
February 12, 2025
Manufacturing Processes
Seed train intensification - the next big step in biopharma?
Seed train intensification is an upstream bioprocessing strategy to improve productivty through modern technologies applying High Cell Density Cryopreservation (HCDC). Learn how seed train intensification can help manufacturers advance production of proteins, such as antibody drug products.
Khalil Essani
November 28, 2024
Manufacturing Processes
Dual Sourcing: Strengthening the Pharmaceutical Supply Chain for Single-Use Assemblies
Dual sourcing strategies select suppliers that can meet quality standards, desired delivery times, and overall price expectations. Vendor-agnostic integrators, like Single Use Support, help provide customized single-use systems tailored to specific client needs. This allows them to select the best components and materials from multiple sources, ensuring compatibility and functionality.
David Seifert
October 28, 2024
Manufacturing Processes
Sustainable Practices: The Green in Single Use Support
As company with “recognition of good performance” Single Use Support has already set ambitious goals for the upcoming years which include to obtain the ISO 14001 certification by 2025 and to reduce emissions by 30% by 2028.
Armin Lassl
September 23, 2024
Manufacturing Processes
Interview with NIBRT: Innovating Freezing & Thawing in Bioprocessing
The collaboration between Single Use Support and the National Institute for Bioprocessing Research and Training (NIBRT) exemplifies a shared commitment to advancing scientific knowledge and driving innovation in the bioprocessing industry.
Michael Eder
August 13, 2024
Manufacturing Processes
Blocking UV Light from Biopharmaceuticals
New on the market are single-use bags that are designed to block ultraviolet (UV) light. By utilizing cold chain packagings that effectively block UV light, manufacturers can maintain the integrity and quality of their products throughout the entire bioprocessing chain.
David Seifert
July 26, 2024
Manufacturing Processes
How to optimize biomanufacturing efficiency
There are several parameters to be considered in the attempt to maximize efficiency in biomanufacturing. In this article, we will discuss different areas that have an impact on process efficiency, including ways to improve them.
Michael Mühlegger
May 13, 2024
Manufacturing Processes
Interview: Efficient Cell Banking in Seed Train Intensification
Khalil Essani, Product Line Manager at Single Use Support, is an expert in bioprocessing applications for single-use technologies. He provides valuable insights in the use of cell banking in seed train intensification.
Khalil Essani
April 4, 2024
Manufacturing Processes
Bubble point test: Purpose & Procedure
Among the possible filter integrity testing methods, the bubble point test belongs to the most frequent ones. Therefore, this article will describe the process along with its applications, benefits and limitations, and its automation.
David Seifert
March 20, 2024
Manufacturing Processes
Annex 1: All you need to know
Annex 1 is a fundamental framework for the production of sterile medicinal goods. This article will provide an overview of the concept, its history, contents, challenges, and perspectives.
Michael Mühlegger
March 20, 2024
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