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\[ \text{AgNO}_3 (aq) + \text{NH}_4\text{SCN} (aq) \rightarrow \text{AgSCN} (s) + \text{NH}_4\text{NO}_3 (aq) \]


After successful clinical trials, the next step involves scaling up the production of the API to meet regulatory standards. This phase is highly regulated by authorities such as the U.S. Food and Drug Administration (FDA) or the European Medicines Agency (EMA), which require extensive documentation regarding the manufacturing process, purity, and stability of the API. Compliance with Good Manufacturing Practices (GMP) is crucial, as it ensures the quality and safety of the pharmaceutical product.


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One of the key challenges in supplementation is ensuring that nutrients are effectively absorbed by the body. Traditional PQQ supplements often face issues related to low bioavailability, meaning that a significant portion of the active ingredient may not be utilized by the cells. This is where liposomal delivery systems come into play.


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