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In the dynamic and complex world of pharmaceuticals and drug development, the quest to find the right Contract Development and Manufacturing Organization (CDMO) often feels akin to searching for a life partner. As a person often facing and meeting the companies scouting for a CDMO I have heard this analogy so many times.  This kind of partner hunt it's a journey filled with careful considerations, weighing options, and seeking that perfect match that aligns with your unique innovation needs. It is a in a way a “do we have the chemistry” test without pointing to the real type of chemistry.  This intricate process, surprisingly like finding a soulmate, requires more than just a scientific approach - it's about understanding, compatibility, and a shared vision.

As the pharmaceutical and biotechnological industries are obliged to align their operations with Good Manufacturing Practice (GMP) guidelines, a unique set of challenges emerges for facilities tasked with producing non-GMP proteins. GMP is widely recognized as the gold standard for ensuring that products are consistently produced and controlled according to quality standards. However, in some cases, the production of non-GMP proteins (or “technical proteins), often required for research, industrial applications, or other non-clinical purposes, becomes a necessity.  At NorthX we serve both the non-gmp and GMP protein communities and place a strong emphasis on utilizing a strong Quality Management System, while at the same time respecting the process for each product.

Are you curious about how DNA plasmids are made? In this article, we guide you through the step-by-step process of constructing these essential genetic tools. We delve into the history and significance of DNA plasmids, as well as the necessary components and techniques involved in their preparation.

The initial phase in the production of cell-based therapies is where innovative ideas are explored and potential therapies are identified. In the dynamic and rapidly evolving field of cell therapy, thorough research and development play a vital role in bringing safe and effective treatments to patients.

DNA sequencing has opened up possibilities for research and medical treatments that were previously unimaginable. Thanks to it, we can improve our understanding of genetics and their role in living organisms, as well as decode genetic information to develop cures for diseases. In this article, we explore what DNA sequencing entails, from how it works to why it matters so much today.

Cell banking is the process of preserving cells for future use, typically for medical treatments or research purposes. It's a relatively new technology that has the potential to revolutionize healthcare. In this article, we explore what cell banking is, how it works, and why it's becoming increasingly important in the field of medicine. Whether you're a healthcare professional or simply curious about the latest advancements in science, this article provides you with a comprehensive understanding of this exciting new technology.

In the pharmaceutical and biotechnology industries, ensuring the safety, quality, and efficacy o products is of paramount importance. Good Manufacturing Practices provide a set of standards and guidelines that must be followed to maintain the integrity of the manufacturing process and guarantee the production of high-quality drugs.

Biologics solutions such as vaccines, gene therapies, and monoclonal antibodies, have revolutionized the pharmaceutical industry, offering innovative solutions for various diseases and conditions.However, with the growing number of biologics companies in the market, it can be overwhelming to narrow down your options and find the one that aligns with your specific needs.

In this article, we’ll guide you through the essential questions you should ask when searching for a biologics company. By asking the right questions, you can gain valuable insights and make an informed decision, ensuring that you collaborate with a company that meets your expectations and goals.