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China has emerged as a powerhouse in the production of APIs, accounting for a significant portion of global supply. One of the primary reasons for this remarkable growth is the country's vast manufacturing capabilities, which benefit from relatively low labor costs and substantial government investment in the pharmaceutical sector. As a result, many Western pharmaceutical companies have increasingly turned to China to source their APIs, leading to a dramatic increase in imports over the past decade.


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Stability testing is a crucial component in the development and quality assurance of both active pharmaceutical ingredients (APIs) and finished pharmaceutical products (FPPs). It ensures that these substances maintain their intended quality, efficacy, and safety during their intended shelf life, providing valuable information to manufacturers and healthcare providers alike.


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Additionally, the global supply chain for APIs has become increasingly complex and interconnected. Many pharmaceutical manufacturers rely on a mix of domestic and international suppliers for their API needs. This globalization presents both opportunities and challenges, including concerns over quality control and intellectual property rights. The COVID-19 pandemic highlighted vulnerabilities within this supply chain, prompting a reevaluation of sourcing strategies and an increased focus on local production capabilities.


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