Nowadays herbal medicines are becoming most popular in the world because globally people desire about natural treatments and the treatment process is syn with the nature. Treatment with medicinal plants is considered as very safe and there is minimal or no side effects. Due to less side effects of the herbal medicines as compared to the allopathic drugs/medicines, the marketing of herbal medicinal products has been gone beyond the expectations. Quality of herbals is a major part of the regulation in which raw materials and finished products specification, analytical and in process methods, stability studies are required. Different countries have different regulatory requirements for the herbal medicinal products. The present manuscript focuses on the classification, regulatory requirements, their comparison and their registration procedure.
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