Last updated on October 7th, 2024 at 05:12 pm
In India, the quality of generic medicines is regulated by the Central Drugs Standard Control Organization (CDSCO), which is the national regulatory authority for pharmaceuticals and medical devices in India. The CDSCO is responsible for ensuring that all medicines, including generic medicines, sold in India meet appropriate standards of quality, safety, and efficacy.
To be approved for sale in India, generic medicines must meet the same standards of quality, safety, and efficacy as their brand-name counterparts. This includes demonstrating that the generic medicine is the same as the brand-name medicine in terms of its active ingredient, dosage form, strength, intended use, and the conditions it is used to treat.
In addition to this regulatory process, generic medicines are also subject to ongoing quality control measures to ensure that they continue to meet these standards throughout their shelf life. This includes testing to ensure that the active ingredients are present in the correct amounts and that the medicine meets other quality standards.
Overall, there are robust systems in place to ensure the quality of generic medicines in India, and they can be a safe and effective treatment option for many people.
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