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The regulatory landscape surrounding APIs is also evolving, with agencies like the FDA and EMA emphasizing the importance of quality and consistency in API production. Recent initiatives aim to streamline the approval process for new APIs while ensuring rigorous safety and efficacy standards. This regulatory support is crucial in bringing innovative therapies to market and ensuring patient safety.


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Moreover, the formulation of pharmaceutical products may also involve consideration of patient populations. For example, certain excipients like lactose may cause adverse reactions in patients with lactose intolerance. As such, manufacturers are increasingly focusing on the selection of excipients that cater to diverse patient needs.


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