I never set out to become the CEO of a Contract Development and Manufacturing Organization (CDMO). Like many things in life, the road to my current position was winding, unpredictable, and—only in hindsight—entirely logical. As a scientist, curiosity has always […]
GMP analytical testing is a core part of bringing a pharmaceutical product to market. Any manufacturing process must produce the right product consistently, and in pharmaceuticals that expectation is reinforced by close regulatory oversight. Products must be manufactured, tested and […]
In the pharmaceutical industry, leadership plays a crucial role in navigating complex challenges and driving a company towards success. Andreas Raabe, our CEO, shares insights into his leadership journey, the values that drive his decisions, and his vision for the […]
Pharmaceutical waste management is a critical topic in the pharmaceutical industry and healthcare settings. With increasing regulations and a growing emphasis on sustainability, understanding how to handle pharmaceutical waste properly is essential. In pharmaceutical manufacturing and CDMO operations, effective pharmaceutical […]
Following the acquisition of one of Japan’s leading pharmaceutical manufacturing facilities, Adragos Pharma launched a large-scale SAP S/4HANA deployment to support digital transformation, operational efficiency, and scalable CDMO manufacturing operations. A critical component of the post-merger integration strategy was aligning […]
In the evolving landscape of the pharmaceutical industry, maintaining high-quality standards is critical for success. At the core of this effort is the Pharmaceutical Quality System (PQS), which ensures that products not only meet regulatory requirements but also serve their […]
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