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High-quality pharmaceutical intermediates must comply with strict regulatory standards. These standards are set by organizations such as the FDA (Food and Drug Administration) and EMA (European Medicines Agency) to ensure the safety and efficacy of medications. The production process involves precise control of various parameters, including temperature, pH, and purity levels. For instance, ethylene glycol diacetate and sodium cumenesulfonate are common intermediates that must be produced under controlled conditions to maintain their quality and effectiveness.

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Once an API has demonstrated its potential through clinical trials, pharmaceutical companies must then ensure that it can be manufactured at scale without compromising its quality. This step often involves the establishment of Good Manufacturing Practices (GMP), which dictate the standards for the production of APIs to guarantee that they meet the necessary quality parameters.


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Vitamin C, or ascorbic acid, is essential for the growth and repair of tissues in the body. It plays a pivotal role in the synthesis of collagen, a protein necessary for skin, cartilage, tendons, ligaments, and blood vessels. Additionally, Vitamin C helps in healing wounds and enhances the immune system’s ability to fight infections. The human body cannot produce or store Vitamin C, emphasizing the need for a consistent supply through diet or supplements.


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