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  • Following the successful completion of pilot manufacturing and quality assurance checks, companies move on to full-scale production. This stage involves the extensive use of reactors, filters, and other industrial equipment to produce the API in large quantities. Everything from raw material sourcing to waste management becomes critical to ensuring not only the quality of the APIs but also the safety and compliance with Good Manufacturing Practices (GMP).


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  • As the demand for clean water continues to rise, understanding the role of chemicals in water purification is paramount. From disinfecting to coagulating and flocculating, the chemicals used in the treatment processes are essential in ensuring the safety and quality of our water supply. While chlorination remains a staple in water treatment, alternative methods like ozonation and the use of hydrogen peroxide are increasingly being explored for their effectiveness and environmental benefits. Careful management of these chemicals is crucial not only to achieve desired purification outcomes but also to safeguard public health and the ecosystem. As we advance in technology and research, the future of water purification will likely see new methods and chemicals that enhance our ability to provide clean and safe drinking water for all.


  • Stability testing is a critical component in the development and approval of active pharmaceutical ingredients (APIs) and finished pharmaceutical products (FPPs). This process involves evaluating how various environmental factors, such as temperature, humidity, and light, affect the quality and efficacy of drugs over time. Understanding stability is vital for ensuring that medications remain safe and effective throughout their shelf life, thus protecting public health.