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Solution
Safe storage of biologics: Requirements & solutions
Once biologics are produced, they need to be stored for shorter or longer periods of time, with dedicated storage requirements to be met. Here, we will uncover these requirements, along with solutions to fulfill them.
Alexander Fuchs
May 8, 2024
Solution
An introduction to therapeutic proteins
Therapeutic proteins hold promise in the treatment of numerous medical conditions, and progress in this field is far from being over. This is reason enough to take a general look at this class of therapeutics.
Alexander Fuchs
April 10, 2024
Solution
Protein storage: How to increase protein stability?
Prior to be used in diagnostics or therapeutics, proteins have to be safely stored. In this article, we will assess methods to preserve their stability upon storage.
Alexander Fuchs
April 10, 2024
Solution
Protein production and optimization strategies
Protein production is a crucial process that which a large variety of pharmaceutical products rely on. Therefore, we will discuss this procedure in this article, along with possibilities to improve it.
Khalil Essani
April 9, 2024
Solution
Protein stability – all you need to know
Protein stability is crucial to be maintained along the manufacturing process of protein-based products. In this article, we will discover what influences protein stability, along with methods to assess and increase it.
Khalil Essani
April 9, 2024
Solution
What are Active Pharmaceutical Ingredients (APIs)?
Active Pharmaceutical Ingredients (APIs) are the cornerstone of pharmaceutical drugs, serving as the primary agents responsible for delivering therapeutic effects to patients.
Michael Eder
March 21, 2024
Solution
Cold Storage Requirements for Active Pharmaceutical Ingredients
Active pharmaceutical ingredients (APIs) are fundamental for drug products to be effective, but require special treatment – e.g. considering humidity, light, or temperature. In this article, we will highlight the different cold storage requirements of APIs, including examples and an overview of different practical approaches.
Alexander Fuchs
March 21, 2024
Solution
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
Solution
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
Solution
Annex 1 and the PUPSIT requirement
Annex 1 and PUPSIT meant significant changes in the pharmaceutical sector. In this article, we will illustrate the focus areas of Annex 1 and will discuss main aspects of PUPSIT.
Khalil Essani
March 13, 2024
Solution
Overview of filter integrity testing methods
There are various approaches to validate the integrity of sterile filters, as is required by several regulatory frameworks. We will cover some of the most common methods in this article.
Khalil Essani
March 13, 2024
Solution
Top 7 pharmaceutical CDMOs in 2024
Progress in the pharmaceutical industry is significantly driven by CDMOs, collaborating with pharma companies. In this article, we will put 7 outstanding CDMOs in the spotlight.
Michael Mühlegger
March 12, 2024
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