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Despite the clear advantages of importing APIs from China, there are notable challenges that pharmaceutical companies must navigate. Regulatory compliance is a significant concern, as the FDA and other regulatory bodies impose strict guidelines on the quality and safety of imported APIs. Companies must conduct thorough due diligence when selecting suppliers to ensure that they comply with Good Manufacturing Practices (GMP) and other international standards.

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In pharmaceuticals, ethylene glycol diformate is being explored as a potential excipient. Its ability to enhance the solubility and bioavailability of certain drugs can lead to more effective therapeutic outcomes. Research into the compound's compatibility with various active pharmaceutical ingredients (APIs) is ongoing, with hopes of establishing EGDF as a standard excipient in drug formulation.

Isoflurane is also associated with environmental and occupational exposure risks, necessitating adherence to safety guidelines. Research facilities must ensure proper ventilation and the use of gas scavenging systems to minimize exposure to staff. Ensuring that these safety protocols are in place not only protects personnel but also meets regulatory standards for animal research.

Safety and Minimal Side Effects

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