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Regulatory agencies, such as the Food and Drug Administration (FDA) and the European Medicines Agency (EMA), require comprehensive stability data as part of the submission process for new drug applications. These entities have established specific guidelines that pharmaceutical companies must follow to ensure that their products meet safety and efficacy standards.

Conclusion

The mechanisms behind photodegradation often involve the absorption of light energy, typically ultraviolet (UV) or visible light. This energy can excite electrons within the API, triggering chemical reactions that break molecular bonds or restructure the compound entirely. Understanding these mechanisms is essential for pharmacists, formulators, and regulatory agencies, as the integrity of the drug must be maintained to ensure patient safety and therapeutic effectiveness.

Chemical Properties

4. Quality Control Before an API can be used in pharmaceuticals, it undergoes rigorous testing to ensure it meets established quality standards. This includes assessments of potency, purity, and stability, as well as additional testing for contaminants.

The Case of l pqq

There are several types of coagulants used in water treatment, with the choice depending on the specific characteristics of the water to be treated. The most widely used coagulants include