Yes, medications, including both branded and generic medications, may have a quality mark on them in India. In India, one of the most common quality marks that is found on medications is the “AYUSH” mark, which stands for “Ayurveda, Yoga and Naturopathy, Unani, Siddha, and Homeopathy.” The AYUSH mark is a quality mark that is used to indicate that a medication has been approved by the Central Council of Indian Medicine (CCIM) or the Central Council of Homoeopathy (CCH), both of which are government agencies responsible for regulating the quality and safety of traditional medicines in India.
In addition to the AYUSH mark, some medications in India may also have other quality marks on them, such as the “IS” mark, which stands for “Indian Standard.” The IS mark is a quality mark that is used to indicate that a medication has been manufactured according to good manufacturing practices (GMPs) and meets the standards for quality and purity set by the Bureau of Indian Standards (BIS), a government agency responsible for setting standards for a wide range of products in India.
Quality Marks Available on Medicines
Here are some examples of quality marks that can be found on medicines:
FDA Approval:
In the United States, the Food and Drug Administration (FDA) is responsible for regulating the quality, safety, and efficacy of medicines. Medicines that have been approved by the FDA typically carry an FDA-approved label or mark on their packaging, indicating that they have met the FDA’s standards for safety and effectiveness.
European Medicines Agency (EMA) Approval:
In Europe, the European Medicines Agency (EMA) is responsible for evaluating and approving medicines for use in the European Union (EU). Medicines that have been approved by the EMA may carry an EMA-approved label or mark on their packaging.
Good Manufacturing Practices (GMP) Certification:
GMP is a set of quality standards that are followed by pharmaceutical manufacturers to ensure that medicines are consistently produced and controlled to meet quality standards. Medicines that are manufactured in facilities that have been certified to comply with GMP may carry a GMP certification mark on their packaging.
Pharmacopeial Standards:
Pharmacopeial standards, such as the United States Pharmacopeia (USP) or the European Pharmacopoeia (Ph. Eur.), provide quality standards for medicines, including specifications for their identity, strength, purity, and quality. Medicines that comply with pharmacopeial standards may carry a pharmacopeial mark or monograph reference on their packaging.
Quality Certification from International Organizations:
Some medicines may carry quality certification marks from international organizations such as ISO (International Organization for Standardization) or WHO (World Health Organization), indicating that they have met certain quality standards.
It’s important to note that the presence of a quality mark on a medicine does not guarantee its safety or efficacy. It’s still important to use medicines as directed by a qualified healthcare professional and follow appropriate dosage instructions and precautions.
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