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After the approved drug is on the market, whether generic or branded, API manufacturers must test each batch of the product according to the identified specifications using validated tests and, with each batch, issue a certificate of analysis (COA) that contains specific test results about the substance

Patient safety is Lillys top priority, and we actively engage in monitoring, evaluating, and reporting safety information for all our medicines

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GLP-1 and Gut Health: Addressing Metabolic Dysfunction Managing metabolic dysfunction is a growing challenge for healthcare providers, but new advances in GLP-1 therapies and gut health optimization offer promising solutions