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Significance of Drug standardization

Drug standardization is a crucial process that establishes the quality, efficacy, and identity of pharmaceutical products. It involves systematic verification to ensure uniformity and safety of medicinal preparations, which is vital for the acceptance of traditional medicines. This procedure also encompasses the quality and authenticity of herbal drugs and Ayurvedic products through consistent measurement and testing. Ultimately, drug standardization confirms a drug's identity, quality, and purity throughout its entire life cycle.

Synonyms: Pharmaceutical standardization, Drug quality control, Pharmaceutical quality assurance, Standard drug formulation

The below excerpts are indicatory and do represent direct quotations or translations. It is your responsibility to fact check each reference.

The concept of Drug standardization in scientific sources

Science Books

Drug standardization is crucial for ensuring the consistency, quality, and safety of medicinal preparations, particularly traditional and herbal medicines, thereby facilitating their global acceptance and ensuring their authenticity through established preparation parameters.

Significance in Scientific journals, articles, etc.:

From: World Journal of Pharmaceutical Research

(1) The process outlined in the study necessary for ensuring the quality and therapeutic efficacy of herbal medicines, including Bacopa monnieri.[1] (2) The process aimed at ensuring the quality, efficacy, and uniformity of pharmaceutical products, especially by systematic verification of their properties.[2] (3) Confirmation of a drug's identity, quality, and purity throughout all phases of its life cycle.[3] (4) The process of establishing the quality, efficacy, and identity of pharmaceutical products.[4] (5) The process of ensuring consistency, quality, and safety of medicinal preparations, which is essential for the global acceptance of traditional medicines.[5]

From: Ancient Science of Life

(1) The process of establishing and maintaining acceptable levels of quality, purity, and potency in medicinal products.[6] (2) The process of ensuring the quality and efficacy of Ayurvedic drugs through consistent measuring and testing methods.[7]

This section includes scientific research in the field of healthcare, often involving traditional medicine systems such as Ayurveda, Unani, Siddha and Holistic health. It includes papers from scientific journals classified as either original, clinical or experimental research, review articles or case reports.