Significance of Pharmaceutical standardization
Pharmaceutical standardization is the systematic process ensuring the quality control, safety, and efficacy of pharmaceuticals, including both conventional and Ayurvedic drugs. This involves establishing uniform criteria for preparation, consistent manufacturing procedures, and rigorous testing protocols to guarantee reproducibility and therapeutic effectiveness. It is essential for the development of high-quality medications, ensuring that formulations meet specific standards, maintain consistent quality, and adhere to safety criteria, ultimately benefiting public health and ensuring reliable medication use.
Synonyms: Drug standardization, Pharmaceutical quality control, Pharmaceutical regulation
The below excerpts are indicatory and do represent direct quotations or translations. It is your responsibility to fact check each reference.
The concept of Pharmaceutical standardization in scientific sources
Pharmaceutical standardization ensures the quality and effectiveness of Ayurvedic medicines by establishing consistent standards for formulations and verifying product quality, as highlighted in research articles on drug efficacy.
From: World Journal of Pharmaceutical Research
(1) The process of establishing consistent criteria for the quality and efficacy of pharmaceutical preparations.[1] (2) The process of ensuring that formulations like Rakta Sthapana Churna maintain consistent quality, safety, and efficacy through proper methods of preparation and testing.[2] (3) The process of ensuring the preparation and quality control of pharmaceuticals, which is essential for drug reproducibility and safety.[3] (4) The process of ensuring that Ayurvedic formulations meet established safety and efficacy criteria to produce high-quality products.[4] (5) An essential process for establishing an efficient drug, focusing on steps from raw material selection to the final product preparation.[5]
From: AYU (Journal of Research in Ayurveda)
(1) Pharmaceutical standardization involves the systematic evaluation and regulation of formulation manufacturing to ensure consistency in quality and efficacy.[6] (2) The process of ensuring consistency in the composition and preparation of Ayurvedic formulations like Chitraka Haritaki Avaleha.[7] (3) The systematic process of developing consistent manufacturing processes and analytical methods for Rajata Sindura.[8] (4) The process of establishing consistent quality and efficacy standards for Ayurvedic formulations and practices.[9] (5) The process of ensuring consistent quality and efficacy in pharmaceutical products, important in Ayurvedic practice.[10]
From: International Ayurvedic Medical Journal
(1) The process of establishing uniform criteria for the preparation and quality control of pharmaceutical products to ensure consistency in their effectiveness.[11] (2) The process of developing standard manufacturing procedures for drugs without compromising their efficacy and safety.[12] (3) The process of establishing consistent and reliable manufacturing procedures for drug preparation, ensuring efficacy and safety.[13] (4) The process of ensuring safety and efficacy in Ayurvedic drug preparations through systematic methods of production and evaluation.[14] (5) The process of ensuring the quality and consistency of a drug formulation, critical for reproducibility and safety.[15]
From: Ancient Science of Life
(1) The process of establishing and maintaining consistency in the quality of pharmaceutical products, specifically in the preparation of Rasasindura.[16] (2) The process of establishing consistent manufacturing procedures and quality control for medications.[17]
From: Ayushdhara journal
(1) The process of ensuring that pharmaceutical formulations meet specific standards of quality and efficacy.[18] (2) The process of ensuring the quality, safety, and effectiveness of Ayurvedic medicines through systematic controls and methodologies.[19]
From: Journal of Ayurveda and Holistic Medicine
(1) The process of establishing and verifying the quality and consistency of pharmaceutical products.[20]
From: Journal of Ayurveda and Integrative Medicine
(1) The process of establishing uniform specifications for the production and quality of Ayurvedic formulations, ensuring consistency in safety and efficacy.[21]