Standardization of Herbal Medicines

Herbal formulations are gradually required out as medicinal products, nutritional supplements and cosmetic in recent years. Herbal medicines originated firstly in the Asian countries and today they are being seen as therapeutic agents for several chronic diseases. Standardization of herbal medicines is the process of prescribing a set of standards or inherent characteristics, constant parameters, definitive qualitative and quantitative values that carry an assurance of quality, efficacy, safety and reproducibility. Herbal drugs are a finished product which is categorised depending upon the ingredients contained in them. Several quality standards as laid down in formularies, pharmacopoeias or manufacturing operation are followed through legal obligatory good manufacturing practices by regulatory authorities.

  • Track 1-1 Herbal drugs
  • Track 2-2 Quality Control and Standardization of Herbal Medicines
  • Track 3-3 Need for Standardization of Herbal formulations
  • Track 4-4 Identity of the drugIdentity of the drug
  • Track 5-5 Physicochemical parameters of the drug
  • Track 6-6 Physicochemical parameters of the drug
  • Track 7-7 Pharmacological parameters
  • Track 8-8 Microbiological contamination
  • Track 9-9 Radioactive contamination
  • Track 10-10 Evaluation methods

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