How has the regulation of pharmaceuticals changed in recent years?

In recent years, the regulation of pharmaceuticals has seen significant changes in California. The California Legislature has enacted multiple laws to ensure the safety, efficacy, and quality of pharmaceuticals available for sale in the state. In 2019, the California Legislature passed a law that expanded the labeling requirements for prescription drugs. This law requires that each prescription medication include information on the maximum recommended dosage and potential adverse reactions. This law also provides guidance to doctors on how to best prescribe medications, as well as an awareness of potential adverse reactions to medications. The California Department of Public Health also recently implemented the California Electronic Laboratory System (CELS). CELS is a web-based system that allows California laboratories to electronically submit quality control sample data to the state. This data is used to ensure that medications meet quality and safety standards. The state also uses this data to track patient safety and consumer complaints regarding the safety and effectiveness of medications. Additionally, the state has implemented new regulation to strengthen the oversight of compounding pharmacies. Compounding pharmacies produce custom medications for patients who cannot take commercially available medications. The new regulation requires compounding pharmacies to register with the state and comply with quality assurance standards in order to remain open. Overall, the state of California has taken steps to ensure that medications available for sale in the state meet high safety and efficacy standards. These new laws and regulations provide an additional layer of protection for patients who are using prescription medications.

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How has the regulation of pharmaceuticals changed in recent years?

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