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Relevant bibliographies by topics / Standardization of drugs

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Journal articles
Dissertations / Theses
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Academic literature on the topic 'Standardization of drugs'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Standardization of drugs"

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Prajapati, Mahindra, Pushpak S. Girase, and Gopal P. Rajput. "Quality Control and Standardization of Herbal Drugs." International Journal of Research Publication and Reviews 4, no. 8 (2023): 2786–99. http://dx.doi.org/10.55248/gengpi.4.823.51870.

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Tambare, Prajakta, Firoj A. Tamboli, and Harinath N. More. "Standardization of herbal drugs: An overview." International Journal of Pharmacognosy and Pharmaceutical Sciences 3, no. 1 (2021): 09–12. http://dx.doi.org/10.33545/27067009.2021.v3.i1a.23.

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Chawre, Sushil Vilas, P. A. Waykar, V. S. Shinde, and J. D. Gulhane. "The Standardization of Daruharidradi Ghanavati." International Journal of Applied & Basic Medical Research 14, no. 1 (2024): 12–16. http://dx.doi.org/10.4103/ijabmr.ijabmr_363_23.

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Abstract Background: Many effective formulations are available in Ayurveda for various diseases. These formulations are lagging in standardization due to the absence of reference standards, whereas maintaining quality standards of given medicines is the need of an hour. Daruharidradi Ghanvati is one such combination of six herbal drugs containing Daruharidra, Meshshrungi, Vijaysar, Mamajjak, Jambubija, and Methikabij. Each drug is described in various Ayurvedic antidiabetic formulations. Aim: The present study was aimed at setting a standard pharmacognostical and pharmaceutical profile of Daru

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Bhusnure, Omprakash G., Shivraj Suryawanshi, S. M. Vijayendra Swamy, Sachin B. Gholve, Padmaja S. Girm, and Mahesh J. Birajdar. "Standardization and Quality Evaluation of Herbal Drugs." Journal of Drug Delivery and Therapeutics 9, no. 3-s (2019): 1058–63. http://dx.doi.org/10.22270/jddt.v9i3-s.2941.

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In recent years most, people throughout world are turning to use medicinal plant and herbal product in healthcare system. the use of herbal product as medicine by the basis of history. The identification of pure active ingredient is an important requirement for Quality and dose determination of plant related dugs. Therefore, evaluation of the parameters based upon chemical, physical, microbiological, therapeutic and toxicological studies can serve as an important tool in stability studies. Standardization of herbal drugs means confirmation of its identity, Quality and purity. The present overv

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Kamboj, Anjoo, Ishtdeep Kaur, and Narinder Kaur. "Recent Advances in Standardization of Herbal Drugs." Current Traditional Medicine 6, no. 4 (2020): 278–99. http://dx.doi.org/10.2174/2215083805666190613141613.

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Background: Herbal drugs play a significant role to maintain the human healthiness and to treat the ailments since the dawn of civilization. Moreover, these plants have provided many lead compounds that culminated in modern medicine. A single herb is regarded as mini-combinatorial library of phytoconstituents hence the quality control of herbal drugs in an herbal formulation is not an easy task because a number of factors impact their pharmacological efficiency and consistent therapeutic effects. Hence, to provide consistent beneficial therapeutic effects, standardized herbal products of consi

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R, Shulammithi, Sharanya M, Tejaswini R, and Kiranmai M. "Standardization and quality evaluation of herbal drugs." IOSR Journal of Pharmacy and Biological Sciences 11, no. 05 (2016): 89–100. http://dx.doi.org/10.9790/3008-11050189100.

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Koshechkin, Konstantin A., B. K. Romanov, and Yu V. Olefir. "STANDARDIZATION OF DESCRIPTION OF MEDICAL PRODUCTS." Medical Journal of the Russian Federation 25, no. 1 (2019): 36–39. http://dx.doi.org/10.18821/0869-2106-2019-25-1-36-39.

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Prerequisites and results of the work carried out by the Scientific Centre for Expert Evaluation of Medicinal Products on the standardization of the values of international non-proprietary, grouping and chemical names of drugs, anatomic-therapeutic-chemical classification, dosage forms, dosage units and other data are presented. The information is reduced to the same unique values in terms of information about identical drugs. This information is required for inclusion in a single directory drugs classifier, created to automate the management of drug purchases and implementation of a system fo

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Nigam, Sarika, Pallavi M. Lavhale, Pankaj Kumar, and Gaurang H. Gupta. "Standardization of Ajmodadichurna and Haritakichurna." INTERNATIONAL JOURNAL OF PHARMACEUTICAL EDUCATION AND RESEARCH (IJPER) 4, no. 02 (2023): 20–24. http://dx.doi.org/10.37021/ijper.v4i2.05.

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Introduction-Standardization is an essential process to evaluate the quality,purity, safety andefficacyof a drug. Standardization meansthecomparison of a test substance with a reference substance on the basis of organoleptic,physical and physiochemical parameters.This article reportson thestandardization ofAjmodadichurnaand Haritakichurna.Ajmodadichurna is a polyherbal classical Ayurvedic medicine containing 12 ingredients. It gives relief in inflammatory painful conditions such as Rheumatism, Sciatica, Neuralgic pain etc. Haritaki is an excellent antioxidant and rejuvenativeherb (Rasayana),ha

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Kardile, Mahendra Vaijnath, Chandaragouda Patil, Ali Haidar, Umesh Bharat Mahajan, and Sameer Goyal. "Homeopathic drug standardization through biological evaluations: An untrodden avenue." International Journal of High Dilution Research - ISSN 1982-6206 14, no. 4 (2021): 16–37. http://dx.doi.org/10.51910/ijhdr.v14i4.768.

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Background: There is a dearth of chemico-analytical or instrumental methods for standardization and quality control of higher dilutions of homeopathic drugs.  Aim: This review highlights the challenges in standardization of anti-inflammatory homeopathic drugs and suggests a battery of biological assays for their standardization. Methods: We retrieved a total 57 scientific reports from the experimental studies and scientific reviews published between January 1999 and June 2014 related to anti-inflammatory homeopathic drugs and their high dilutions. These comprised of 18 reports on p

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Desai, Sonal, and Pratima Tatke. "Phytochemical Markers: Classification, Applications and Isolation." Current Pharmaceutical Design 25, no. 22 (2019): 2491–98. http://dx.doi.org/10.2174/1381612825666190709203239.

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Background: There has been aroused demand for herbal drugs/products worldwide because of their fewer side effects as compared to synthetic drugs. The major obstacle in the global acceptance of herbal products is the lack of proper standardization technique. Methods: Various test procedures have been used for authentication and quality control of botanicals among which marker based standardization has attained more attention. The major challenge faced by phytochemist is to select appropriate phytochemical marker for quality control of herbal drugs. Phytochemical markers used for standardization

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Dissertations / Theses on the topic "Standardization of drugs"

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Nel, Hanri. "The establishment and standardization of a veterinary antimicrobial resistance programme in South Africa." Diss., University of Pretoria, 2001. http://upetd.up.ac.za/thesis/available/etd-03092005-083138/.

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Lindkvist, Daniel, and Siet-ling Law. "Standardisering av hjälpmedel för sjuksköterskor." Thesis, KTH, Hållbar produktionsutveckling (ML), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-276730.

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Syftet med detta projekt var att identifiera om en implementering av en standardisering för receptbelagda läkemedelsförpackningar, skulle kunna bidra till en minskad risk gällande feldosering eller felmedicinering av patient. Resultatet av studien konstaterar att en standardisering för ordinationer har större effekt.<br>The purpose of this project was to identify if an implementation of a standardization for prescription drugs packaging, could contribute to a reduced risk of error when medicating a patient with prescription drugs and dosage. The outcome of the study states that a standardizati

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Jonvallen, Petra. "Testing Pills, Enacting Obesity : The work of localizing tools in a clinical trial." Doctoral thesis, Linköping : Univ. Department of Technology and Social Change, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-5132.

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Jeon, Hyae Won Jennifer. "Standardization and use of colour for labelling of injectable drugs." Thesis, 2008. http://hdl.handle.net/10012/3764.

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Medication errors are one of the most common causes of patient injuries in healthcare systems. Poor labelling has been identified as a contributing factor of medication errors, particularly for those involving injectable drugs. Colour coding and colour differentiation are two major techniques being used on labels to aid drug identification. However, neither approach has been scientifically proven to minimize the occurrence of or harm from medication errors. This thesis investigates potential effects of different approaches for using colour on standardized labels on the task of identifying

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Books on the topic "Standardization of drugs"

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WHO Expert Committee on Biological Standardization. and World Health Organization, eds. WHO Expert Committee on Biological Standardization: Fiftieth report. World Health Organization, 2002.

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WHO Expert Committee on Biological Standardization., ed. WHO Expert Committee on Biological Standardization: Thirty-seventh report. World Health Organization, 1987.

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Organization, World Health, ed. WHO Expert Committee on Biological Standardization: Forty-ninth report. World Health Organization, 2000.

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WHO Expert Committee on Biological Standardization., ed. WHO Expert Committee on Biological Standardization: Thirty-eighth report. World Health Organization, 1988.

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WHO Expert Committee on Biological Standardization. and World Health Organization, eds. WHO Expert Committee on Biological Standardization: Forty-sixth report. World Health Organization, 1998.

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WHO Expert Committee on Biological Standardization. and World Health Organization, eds. WHO Expert Committee on Biological Standardization: Forty-seventh report. World Health Organization, 1998.

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WHO Expert Committee on Biological Standardization. and World Health Organization, eds. WHO Expert Committee on Biological Standardization: Forty-eighth report. World Health Organization, 1999.

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WHO Expert Committee on Biological Standardization. WHO Expert Committee on Biological Standardization: Fortieth report. World Health Organization, 1990.

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Organization, World Health, and ebrary Inc, eds. WHO Expert Committee on Biological Standardization: Fifty-sixth report. World Health Organization, 2007.

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WHO Expert Committee on Biological Standardization., ed. WHO Expert Committee on Biological Standardization: Thirty-sixth report. World Health Organization, 1987.

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Book chapters on the topic "Standardization of drugs"

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Al-Harrasi, Ahmed, Saurabh Bhatia, Deepak Kaushik, Tapan Behl, and Sridevi Chigurupati. "Standardization and Quality Control of Crude Drugs." In Recent Advances in Natural Products Science. CRC Press, 2022. http://dx.doi.org/10.1201/9781003274124-6.

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Rajani, M., and Niranjan S. Kanaki. "Phytochemical Standardization of Herbal Drugs and Polyherbal Formulations." In Bioactive Molecules and Medicinal Plants. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-74603-4_19.

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Sharma, Arun K., Bitasta Mandal, Swati Madan, and Satyendra K. Rajput. "Challenges and Opportunities in Standardization of Homeopathic Drugs and Dilutions." In Herbal Medicine in India. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7248-3_36.

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Alamgir, A. N. M. "Herbal Drugs: Their Collection, Preservation, and Preparation; Evaluation, Quality Control, and Standardization of Herbal Drugs." In Progress in Drug Research. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-63862-1_10.

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Husser, Casey S., Jeffrey R. Buchhalter, O. Scott Raffo, et al. "Standardization of Microarray and Pharmacogenomics Data." In Bioinformatics and Drug Discovery. Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-964-8:111.

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Garg, Vandana, Ghazala Zia, Mahima Chauhan, and Rohit Dutt. "Facts about Standardization of Herbal Medicines." In Promising Drug Molecules of Natural Origin. Apple Academic Press, 2020. http://dx.doi.org/10.1201/9781003010395-2.

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Morbelli, Silvia, and Matteo Bauckneht. "Amyloid PET Imaging: Standardization and Integration with Other Alzheimer’s Disease Biomarkers." In Biomarkers for Alzheimer’s Disease Drug Development. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7704-8_13.

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Stacey, Glyn N., and Thomas Hartung. "Availability, Standardization and Safety of Human Cells and Tissues for Drug Screening and Testing." In Drug Testing in vitro. Wiley-VCH Verlag GmbH & Co. KGaA, 2006. http://dx.doi.org/10.1002/9783527609611.ch9.

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Maeki, Masatoshi, and Manabu Tokeshi. "Engineered and Artificial Exosomes for Non-viral Drug Delivery Nanocarriers." In Extracellular Fine Particles. Springer Nature Singapore, 2025. https://doi.org/10.1007/978-981-97-7067-0_19.

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Abstract This chapter overviews the expanding field of engineered and artificial exosomes as cutting-edge non-viral drug delivery nanoparticles. Exosomes are expected to be natural carriers for drug delivery systems and clinical trials are in progress for several exosome-based nanomedicines. While therapeutic potential of exosomes has been demonstrated, several challenges must be overcome for practical applications including the need for: scalable manufacturing, standardization, and efficient drug loading. To overcome them, various methodologies have been developed for the production of engine

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Pharmacista, Gandhi, and Virly Vidiasti Sabijanto. "Protection of Drug Raw Materials Through Price Standardization as a Business Rule in Supporting Competitive Local Drug Production." In Proceedings of the 3rd International Conference on Business Law and Local Wisdom in Tourism (ICBLT 2022). Atlantis Press SARL, 2023. http://dx.doi.org/10.2991/978-2-494069-93-0_81.

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Conference papers on the topic "Standardization of drugs"

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Singh, Shalini, and Krishnan Kanny. "Harmonizing Design, Risk, Metrology and Standardization in Managing the Development of Drugs using Nanotechnology." In 4th African International Conference on Industrial Engineering and Operations Management. IEOM Society International, 2023. http://dx.doi.org/10.46254/af04.20230095.

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de Lacerda, Dhiego Alves, Pedro Fechine Honorato, Larissa Luana Lopes Lima, et al. "Strategies for reducing costs in anesthesia: Examples of successful initiatives in Brazilian health institutions." In VI Seven International Multidisciplinary Congress. Seven Congress, 2024. http://dx.doi.org/10.56238/sevenvimulti2024-111.

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This paper reviews strategies adopted by health institutions in Brazil to reduce costs in anesthesia services. The initiatives include the standardization of protocols, the use of generic drugs and the optimization of material resources. Results demonstrate that such measures are effective in reducing operating costs, without compromising the quality and safety of anesthetic services. Managers are encouraged to consider these practices to sustain financial efficiency and improve hospital care.

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Hoppensteadt, D., J. Fareed, J. M. Walenga, R. M. Emnuele, and A. Racanelli. "DIFFERENT LOW MOLECULAR WEIGHT HEPARINS (LMWHs) ARE NOT IDENTICAL IN THE IN VITRO SCREENING REGARDLESS OF POTENCY ADJUSTMENT." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643227.

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There is considerable controversy in the standardization and potency evaluation of low molecular weight heparins (LMWHs).Since these agents are produced by fractionation or depolymerization procedures, the resulting material shows marked compositional variations regardless of the similarity in molecular weight. In order to address the question “are different LMWHs the same?”, we utilized a uniform multiparametric in vitro test battery. Seven commercial LMWHs Choay Fraxiparine (CY 216), Choay CY 222, Novo LHN, Kabi Fragmin, Opocrin 2123 (OP), Hepar RD 11885 (RD), Pharmuka Enoxaparine (PK) and a

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dos Santos, Adriano, Silvana Andreia Molina Lima, Marcia Cercal Fernandes, and Simone Fernanda Gonçalves. "The importance of pharmacovigilance notifications in a teaching hospital: Experience report." In VI Seven International Multidisciplinary Congress. Seven Congress, 2024. http://dx.doi.org/10.56238/sevenvimulti2024-087.

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Pharmacovigilance is an important activity for society. It contains a complex regiment in the hospital environment that aims at total patient safety as well as the analysis of problems related to the use of medications, risks that can be harmful to health during the hospitalization process. There are numerous errors in the use of medications, so applying the risk management tool in the establishment can be an alternative to ensure a safe process. In order to create risk prevention strategies, it is important to identify and analyze the causes of events and implement preventive actions before a

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Jelisic, Elena, Nenad Ivezic, Boonserm Kulvatunyou, Perawit Charoenwut, and Ana Nikolov. "An Investigation Into an Approach for Automated Supply Chain Onboarding." In ASME 2023 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/detc2023-117486.

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Abstract The COVID-19 pandemic has brought the cold chain for biopharmaceutical products to the spotlight. To preserve their structure and function, biopharmaceuticals such as cells, proteins and enzymes, RNA molecules, and RNA-based drugs (e.g., mRNA-based COVID-19 vaccines) require low temperatures for proper handling, storage, and transport. Due to the sensitivity of these products transported through cold chains and the lack of traceability, risks associated with the stability, efficacy, safety, tardiness, quality, and waste are significant. For this reason, the ability to quickly find, co

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Dudnic, Eugeniu, and Natalia Dudnic. "Anti-doping control in sport." In The International Scientific Congress "Sports. Olimpysm. Health". SOH 2023. 8th Edition. The State University of Physical Education and Sport, 2025. https://doi.org/10.52449/soh23.17.

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Anti-doping control encountered complicated problems, such as obtaining a consensus on the definition of doping, distinguishing doping from legitimate medical treatment, establishing the evidence of a doping case. At the same time, the proposals for solving these problems often conflicted with national or international laws, so that a lack of standardization in the procedures was manifested. In 1990, the Council of Europe adopted the Anti-Doping Convention, in which 28 EU member countries participate. The main achievement of the convention is that it obliges governments to adopt minimum standa

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Laury, Renard. "Standardization of heroic drug formulas: international agreements of 1906 and 1925." In 46th INTERNATIONAL CONGRESS FOR THE HISTORY OF PHARMACY. Pharmaceutical Association of Serbia, 2024. http://dx.doi.org/10.46793/ishp46.145l.

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Mansani, Fabio Postiglione, Mariane Marcelino Fernandes, Mario Rodrigues Montemor Netto, and Cristiane da Costa Bandeira Abrahão Nimir. "COMPARATIVE ANALYSIS BETWEEN IMMUNOHISTOCHEMISTRY PATHOLOGICAL SUBTYPING AND MAMMAPRINT® GENETIC SIGNATURE IN PATIENTS WITH BREAST CANCER IN BRAZIL: A PILOT STUDY." In Abstracts from the Brazilian Breast Cancer Symposium - BBCS 2021. Mastology, 2021. http://dx.doi.org/10.29289/259453942021v31s2098.

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Introduction: Immunohistochemistry, in breast cancer samples, measures the expression of biomarkers such as estrogen receptor (ER), progesterone receptor (PR), HER2, and Ki67. Using the positivity or negativity of the receptors and the Ki67 value, this method, along with the histological results, allows the doctors to classify the tumors into four types as follows: Luminal A, Luminal B, HER2, and basal/triple negative. Genetic signature is a tool involving in numerous studies in this area; however owing to the difficulty of access to the tests, its usefulness is still limited. MammaPrint® was

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Palagi, Kristopher. "Weaving a Logic of Assembly." In 2017 ACSA Annual Conference. ACSA Press, 2017. http://dx.doi.org/10.35483/acsa.amp.105.25.

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Concrete formwork is expensive. Within residential construction, the wood installed, shed and discarded compounded by the exhaustive cost of labor, make casting even a simple straight wall insurmountable. Regardless of the number of sustainable practices thrown at it — engineered, reclaimed, recycled — to attempt a novel form becomes an unjustifiable venture. Moving away from wood, prefabricated formwork can minimize the cost but drags along baggage of its own. Metal panels demand a strict adherence to standardization for efficiency, while foam blocks only allow the structural integrity to ble

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Nassau, Christopher J., Timothy J. Wray, and Ramesh K. Agarwal. "Computational Fluid Dynamic Analysis of a Blood Pump: An FDA Critical Path Initiative." In ASME/JSME/KSME 2015 Joint Fluids Engineering Conference. American Society of Mechanical Engineers, 2015. http://dx.doi.org/10.1115/ajkfluids2015-26131.

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Computational Fluid Dynamics (CFD) has become a routine tool in recent times for use in blood-contacting medical device design and analysis, such as prosthetic heart valves and ventricular assist devices (VADs). While CFD can aid in design by decreasing the need for expensive prototyping and iterative laboratory testing, standardizations are not currently available for CFD to be used for medical device safety analysis at the preclinical stage. To address this, the U.S. Food and Drug Administration (FDA)’s Center of Devices and Radiological Health (CDRH) has sponsored CFD “round-robins.” This p

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