Relevant bibliographies by topics / Analytical Method Development and Validation

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Analytical Method Development and Validation'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Analytical Method Development and Validation"

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Helaskar, Chandrashekhar Bhagvatrao, and S. R. Kulkarni. "Analytical method development and validation for Aluminium." International Journal of Research and Development in Pharmacy & Life Sciences 7, no. 4 (2018): 3034–38. http://dx.doi.org/10.21276/ijrdpl.2278-0238.2018.7(4).3034-3038.

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Mukesh, Patil* Roshani Dhumal Ashish Jain Srushti Kadave Aishwarya Patil. "A Review: Analytical Method Development and Validation." International Journal of Pharmaceutical Sciences 2, no. 12 (2024): 2350–65. https://doi.org/10.5281/zenodo.14506358.

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In the process of finding new drugs, analytical development and validation are crucial. It is a continuous and inter-dependent task linked with research and development, quality assurance and quality control department. Analytical method development and validation helps to demonstrate that the technique developed it precise, accurate, linear, and robust, as well as specific to analyse a drug in pharmaceutical industry. The essential part of a study is developing the analytical methodology. Advancement in analytical instruments lead to recent development in analytical methods. The excipients, a
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Singh, Jitender, Sonia Sangwan, Parul Grover, Lovekesh Mehta, Deepika Kiran, and Anju Goyal. "Analytical Method Development and Validation for Assay of Rufinamide Drug." Journal of Pharmaceutical Technology, Research and Management 1, no. 2 (2013): 191–203. http://dx.doi.org/10.15415/jptrm.2013.12012.

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Swati, Raysing, Patil Mansi, and Patil Aditya. "Analytical Method Development and Validation: A Concise Review (Review Article)." International Journal of Pharmacy and Biological Sciences 11, no. 1 (2021): 09–16. http://dx.doi.org/10.21276/ijpbs.2021.11.1.2.

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A Patel, Sachin. "A Review on Analytical Method Development and Validation for Lusutrombopag." International Journal of Science and Research (IJSR) 12, no. 4 (2023): 1321–23. http://dx.doi.org/10.21275/sr23419114521.

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Prajakta, G.Thete* and Ravindra B. Saudagar. "REVIEW ON ANALYTICAL METHOD DEVELOPMENT AND VALIDATION BY RP-HPLC." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES 05, no. 05 (2018): 4897–907. https://doi.org/10.5281/zenodo.1286144.

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Analytical method development, validation, and transfer are essential elements of any pharmaceutical development program. Effective method development confirms that laboratory resources are optimized, while methods meet the objectives required at each stage of drug development. High performance liquid chromatography is most accurate methods extensively used for the qualitative and quantitative analysis of drug product. Analytical method development and validation play vital role in the drug discovery, Drug development and manufacture of pharmaceuticals. It includes detection of the purity and
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Vijaya, Kumar Meher, Gautam Girendra, Prasad Meher Chaitanya, and Kumar Patro Saroja. "A Recent Review On Analytical Method Development and Validation." American Journal of PharmTech Research 12, no. 5 (2022): 49–65. https://doi.org/10.5281/zenodo.7270167.

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ABSTRACT In this review articles, the development, formulation, and manufacture of drugs, analytical method development & validation play a critical role. Methods are developed for ensuring purity, identity, potency, and performance of pharmaceutical products. Methods should be applied to the extent that they are sufficient for their intended purpose. Throughout the life cycle of a drug product and substance, a range of activities are associated with developing and validating methods. An objective of method validation is to prove that the procedure can be used as intended. Once the method
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Mohd., Ibrahim, Goyal Rakesh, and Agarwal Dilip. "DEVELOPMENT AND VALIDATION BY HPLC METHOD." International Journal of Current Pharmaceutical Review and Research 14, no. 03 (2022): 104–7. https://doi.org/10.5281/zenodo.12658787.

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Validation of an analytical procedure is the process of demonstrate with suitable for itsintended purpose. Chromatographic such HPLC methods play significant role in thepharmaceutical industry from the drug discovery, development of drugs, formulations andquality control of chemicals. Many validated analytical methods ensure that it providesconsistent, reliable and accurate data for results. So these methods help pharmaceuticalanalyst to ensure quality products are released for market. This review explains generalapproach for validation process and validation parameters to be considered during
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Shashi, Daksh, and Goyal Anju. "Analytical Method Development and Validation: A Review." Chemistry Research Journal 5, no. 3 (2020): 173–86. https://doi.org/10.5281/zenodo.12589409.

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<strong>Abstract </strong>This review focuses on approach to the validation of HPLC method with the compliance of restrictive needs and accepted pharmaceutical practices. The information during this review provides the explanations for performing analytical method validation. The validation parameters needed to be performed in validation for assay and organic impurities strategies. Individual validation parameters are mentioned in reference to the kind of method such assay and organic impurities method to be valid. This review was written to assist chemists/analysts to perform for method valid
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VLN, SAGAR, SHARMA GVR, OMPRAKASH G, and BHARAT KB. "ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR RELATED SUBSTANCE IN OLANZAPINE BY HPLC." Indian Research Journal of Pharmacy and Science 3, no. 3 (2016): 763–72. http://dx.doi.org/10.21276/irjps.2016.3.3.5.

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Dissertations / Theses on the topic "Analytical Method Development and Validation"

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Brown, Jared R. "Analytical Methods Development for High-Throughput Photochemisty With Led Arrays." Thesis, Virginia Tech, 2007. http://hdl.handle.net/10919/32709.

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This thesis describes the design, construction, and evaluation of a series of LED array photolysis systems for high throughput photochemistry. Three generations of array systems of increasing sophistication are evaluated using calorimetric measurements and potassium tris(oxalato)ferrate(III) chemical actinometry. The results are analyzed using descriptive statistics and analysis of variance (ANOVA). The LEDs in the third generation array were shown to be statistically equivalent, with respect to light output, according to physical and chemical actinometry experiments. The third generation
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Malm, Mikaela. "Drug Analysis : Bioanalytical Method Development and Validation." Doctoral thesis, Uppsala universitet, Analytisk kemi, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-8547.

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This thesis describes bioanalytical methods for drug determination in biological matrixes, with drugs in focus used against diseases largely affecting low-income countries. Solid-phase extraction is used for sample cleanup, and processed samples are analyzed by liquid chromatography. Developed bioanalytical methods are validated according to international guidelines. Eflornithine (DFMO) is a chiral drug, used for treating human African trypanosomiasis. A bioanalytical method for determination of DFMO enantiomers in plasma is presented. The enantiomers are detected by evaporative light-scatteri
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Lindholm, Johan. "Development and Validation of HPLC Methods for Analytical and Preparative Purposes." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, Univ.-bibl. [distributör], 2004. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-4442.

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Pingeon, Marine. "Development and validation of analytical methods for therapeutic drug monitoring." Doctoral thesis, Universita degli studi di Salerno, 2019. http://elea.unisa.it:8080/xmlui/handle/10556/4509.

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2017 - 2018<br>The U.S. Food and Drug Administration defines as Precision or Personalized Medicine (PM) an innovative therapeutic approach that tailors therapy and prevention on patients based on inter-individual variabilities in molecular or environmental features and in lifestyles. The major goals of PM are to maximize treatment efficacy and to reduce cost, toxicities and therapy failure rates by early identification of patients who might benefit or not of a specific treatment. In this scenario, therapeutic drug monitoring (TDM) is an important laboratory tool for PM because of the poss
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Holman, Miranda K., Dorcas Frempong, Stacy Brown, Steven Dinh, and Ashana Puri. "Development and Validation of a Liquid Chromatography-Mass Spectrometry Based Analytical Assay for Determination of Cromolyn Sodium in Skin Permeation Studies." Digital Commons @ East Tennessee State University, 2021. https://dc.etsu.edu/asrf/2021/presentations/45.

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Cromolyn sodium (CS) is a mast cell stabilizer which has been used to treat systemic mastocytosis, allergic- and exercise-induced asthma, and allergic reactions induced by atopic dermatitis. Presently, CS is administered orally and intranasally, and with a short half-life and poor absorption, 4 to 8 doses are required daily for treatment. Developing a transdermal product for CS would eliminate such drawbacks that lead to inconsistent patient dosing and provide sustained therapeutic effects when administered via skin. Our long-term goal is to determine the feasibility of delivering CS through s
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Jonsson, Ann-Sofie. "Development and Validation of a Liquid Chromatography-Tandem Mass Spectrometry Method for Determination of Cyclosporine A in Whole Blood." Thesis, Karlstad University, Division for Chemistry, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:kau:diva-5511.

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<p>Cyklosporin A (CsA) är en cyklisk polypeptid med molekylvikten är 1202.6 Da. Substansen har svampursprung (<em>Tolypocladium inflatum Gams)</em> och starka immunhämmande egenskaper. CsA används därför som immunsuppressivt läkemedel för att förhindra avstötning av transplanterade organ och benmärg, samt vid behandling av graft-versus-host-disease (transplantat-mot-värd-sjukdom). CsA har ett snävt terapeutiskt fönster, vilket betyder att skillnaden mellan effektivitet och toxicitet är liten. Biverkningarna av substansen är många och en del av dem allvarliga, såsom nedsatt njurfunktion och öka
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Amann, Laura. "Development and Validation of an Analytical Method for Phenolic Acid Extraction from Cereals and Quantification using HPLC-UV." Thesis, Linnéuniversitetet, Institutionen för kemi och biomedicin (KOB), 2018. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-77227.

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Cereals are rich in phenolic acids, a group of secondary plant metabolites that are associated with reduced risk of chronic diseases. The objective was to develop and internally validate a method for extraction and quantification of phenolic acids in cereals using HPLC-UV and to apply this method for quantification of the content of phenolic acids in several species of Swedish cereals. Different procedures for extraction of phenolic acids from cereal grains using acid or base hydrolysis with and without subsequent enzymatic treatment were tested. Both the extraction procedure and the chromatog
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Persson, Emelie. "Development and validation of a method for separation of pregabalin and gabapentin capsules using Near Infrared hyperspectral imaging." Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-161108.

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Seizures containing large numbers of units of narcotics, goods dangerous to health and doping are often sent to the Swedish National Forensic Centre (NFC). Only a fraction of these capsules or tablets can be analyzed, therefore the samples need to represent the whole seizure. If the samples show content variations, Near Infrared (NIR) spectroscopy in combination with hyperspectral imaging has been shown to be a promising tool to gauge the homogeneity in the seizures based on chemical content. The objective of this thesis was to further develop and then validate a method for the separation of p
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Jackson, Remonica, Mariah Huskey, and Stacy Brown. "Development and validation of a liquid chromatography-tandem mass spectrometric method for quantification of nicotine in e-cigarette liquids." Digital Commons @ East Tennessee State University, 2019. https://dc.etsu.edu/asrf/2019/schedule/238.

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Introduction. Popularity of electronic cigarettes (e-cigarettes) has increased dramatically in recent years, especially among adolescents. The most recent data from the National Institute on Drug Abuse (NIDA) cites that >16% of 12th graders have tried e-cigarettes, and >30% of those individuals will start smoking within 6 months1. E-cigarettes are available in a variety of ‘strengths’ indicating the labeled nicotine concentration in the product. In this project, we sought to investigate the accuracy of nicotine labeling found in some commercially available e-liquids. As such, we developed and
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Arnell, Robert. "Development and Validation of Methods for Characterization of Multi-Component Systems in Preparative LC." Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-7422.

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Books on the topic "Analytical Method Development and Validation"

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1940-, Krull Ira S., ed. Analytical method development and validation. M. Dekker, 1997.

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M, Riley Christopher, and Rosanske Thomas W, eds. Development and validation of analytical methods. Pergamon, 1996.

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Chan, Chung Chow, Herman Lam, Y. C. Lee, and Xue-Ming Zhang, eds. Analytical Method Validation and Instrument Performance Verification. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471463728.

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Chow, Chan Chung, ed. Analytical method validation and instrument performance verification. Wiley-Interscience, 2004.

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Chow, Chan Chung, Lam Herman, and Zhang Xue-Ming, eds. Method validation and instrument performance verification for advanced analytical techniques. Wiley, 2010.

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D, Estes Eva, and Atmospheric Research and Exposure Assessment Laboratory (U.S.), eds. Development and validation of a test method for formaldehyde emissions. U.S. Environmental Protection Agency, Atmospheric Research and Exposure Assessment Laboratory, 1990.

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E, Walker Richard, and United States. National Aeronautics and Space Administration., eds. LOX/Hydrocarbon rocket engine analytical design methodology development and validation: Final report. National Aeronautics and Space Administration, 1993.

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E, Walker Richard, and United States. National Aeronautics and Space Administration., eds. LOX/Hydrocarbon rocket engine analytical design methodology development and validation: Final report. National Aeronautics and Space Administration, 1993.

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James, H. A. Development of an analytical method for blue-green algal toxins. National Rivers Authority, 1991.

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R, Kennedy Eugene, and National Institute for Occupational Safety and Health. Division of Physical Sciences and Engineering., eds. Guidelines for air sampling and analytical method development and evaluation. U.S. Dept. of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, Division of Physical Sciences and Engineering, 1995.

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Book chapters on the topic "Analytical Method Development and Validation"

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Incledon, Chantal, and Herman Lam. "Development and Validation of Automated Methods." In Analytical Method Validation and Instrument Performance Verification. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471463728.ch5.

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Kapetanovic, Izet M., and Alexander V. Lyubimov. "Analytical Chemistry Methods: Developments and Validation." In Preclinical Development Handbook. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470249031.ch5.

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Brandt, Peter. "Development and validation of analytical methods." In Bericht aus dem Nationalen Referenzlabor des BVL für das Jahr 2008. Birkhäuser Basel, 2009. http://dx.doi.org/10.1007/978-3-0346-0235-8_2.

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Hout, Sam A. "Analytical Methods Development, Validation, and Transfer." In Manufacturing of Quality Oral Drug Products. CRC Press, 2022. http://dx.doi.org/10.1201/9781003224716-21.

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Chan, Chung Chow, and Eric Jensen. "Overview of Pharmaceutical Product Development and Its Associated Quality System." In Analytical Method Validation and Instrument Performance Verification. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471463728.ch1.

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Chan, Chung Chow. "Potency Method Validation." In Analytical Method Validation and Instrument Performance Verification. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471463728.ch2.

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Chan, Chung Chow, Neil Pearson, Anna Rebelo-Cameirao, and Y. C. Lee. "Dissolution Method Validation." In Analytical Method Validation and Instrument Performance Verification. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471463728.ch4.

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Garofolo, Fabio. "Bioanalytical Method Validation." In Analytical Method Validation and Instrument Performance Verification. John Wiley & Sons, Inc., 2004. http://dx.doi.org/10.1002/0471463728.ch8.

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Reichenbächer, Manfred, and Jürgen W. Einax. "Validation of Method Performance." In Challenges in Analytical Quality Assurance. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-16595-5_5.

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Burgess, Christopher, R. D. McDowall, and Hermann Wätzig. "Analytical Instrument Qualification." In Method Validation in Pharmaceutical Analysis. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527672202.ch2.

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Conference papers on the topic "Analytical Method Development and Validation"

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Sirbu, Rodica. "DEVELOPMENT AND VALIDATION OF ANALYTICAL METHOD FOR THE QUANTITATIVE DETERMINATION OF NEUROLEPTIC PRODUCT." In 17th International Multidisciplinary Scientific GeoConference SGEM2017. Stef92 Technology, 2017. http://dx.doi.org/10.5593/sgem2017/61/s25.082.

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Deceuninck, Sharon, Mia Loccufier, Wim De Waele, Kris Hectors, and Hans De Backer. "Development and validation of a train-bridge interaction model." In IABSE Symposium, Manchester 2024: Construction’s Role for a World in Emergency. International Association for Bridge and Structural Engineering (IABSE), 2024. http://dx.doi.org/10.2749/manchester.2024.0190.

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&lt;p&gt;In this paper, a train-bridge interaction model is presented to simulate the behaviour of a bridge during the passage of a train. Two modelling methods are compared: the direct integration method (DIM) and the intersystem iteration method (ISIM). First, a simply supported bridge subjected to a moving spring-mass is modelled using both methods and validated with an analytical solution. Subsequently, incorporating damping into the model adds an extra layer of complexity, rendering the search for analytical solutions unfeasible. The validation of the more complex models is accomplished b
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Zhang, Dongyang, Jianjun Liu, and Hongde Jiang. "The Development and Validation of Fast Numerical Method of Simulating Wet Steam Flow." In ASME 2002 Pressure Vessels and Piping Conference. ASMEDC, 2002. http://dx.doi.org/10.1115/pvp2002-1585.

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A fast numerical method of simulating turbine nucleating flow is developed and calibrated. Analytical limiting subcooling degree, transition function and tabular steam properties are applied. The agreements between calculations and experimental data are well. The developed method applies some new and unique techniques and is contributed to be a tool of fast analysis and industrial design for wet steam flow.
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van Geel, M. H. A., C. G. Giannopapa, and B. J. van der Linden. "Development of a Blood Flow Model and Validation Against Experiments and Analytical Models." In ASME 2010 Pressure Vessels and Piping Division/K-PVP Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/pvp2010-26150.

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In cardiovascular research, FSI is expressed by the interaction of the blood with the vessel or the heart. FSI plays a crucial role when the deformation of the boundary, in this case the vessel wall, cannot be neglected. Arterial blood flow and wave propagation in liquid filled vessels has been investigated by many researchers. Their work comprises computational, theoretical and experimental investigations and will be outlined below. This paper presents the development and validation of an arterial blood flow model. The model has been developed using finite elements and the fluid and the solid
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van Geel, M. H. A., C. G. Giannopapa, B. J. van der Linden, and J. M. B. Kroot. "Development of a Blood Flow Model Including Hypergravity and Validation Against an Analytical Model." In ASME 2010 Pressure Vessels and Piping Division/K-PVP Conference. ASMEDC, 2010. http://dx.doi.org/10.1115/pvp2010-26149.

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Fluid structure interaction (FSI) appears in many areas of engineering, e.g. biomechanics, aerospace, medicine and other areas and is often motivated by the need to understand arterial blood flow. FSI plays a crucial role and cannot be neglected when the deformation of a solid boundary affects the fluid behavior and vice versa. This interaction plays an important role in the wave propagation in liquid filled flexible vessels. Additionally, the effect of hyper gravity under certain circumstances should be taken into account, since such exposure can cause alterations in the wave propagation unde
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Sallé, A., J. Fouillet, C. Donzé, L. Rubira, and C. Fersing. "3PC-040 Radiochemical purity determination of 177Lu-PSMA-617: development and validation of a high-performance liquid chromatography analytical method." In 28th EAHP Congress, Bordeaux, France, 20-21-22 March 2024. British Medical Journal Publishing Group, 2024. http://dx.doi.org/10.1136/ejhpharm-2024-eahp.97.

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Checcacci, Damaso, Riccardo Ferraro, Gabriele Girezzi, Nicola Mitaritonna, and Claudio Orazi. "Development and Experimental Validation of a Model-Based Balancing Prediction Method for Bowed Rotor." In ASME Turbo Expo 2023: Turbomachinery Technical Conference and Exposition. American Society of Mechanical Engineers, 2023. http://dx.doi.org/10.1115/gt2023-103686.

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Abstract Rotor balancing is one of the most discussed topics in the field of rotor-dynamics. It is very important in the industrial practice and sometimes there are very particular cases that cannot be addressed and solved by traditional methods. The rotor model addressed in this paper has been initially presented in a previous work [1], with the aim to introduce a procedure for “predicting the effects of balancing” at rotational speeds that are higher than those possible on balancing machines. In this work, the balancing of the same rotor model is addressed by a maintenance standpoint, consid
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Rezaei, M. M., M. R. Movahhedy, M. T. Ahmadian, and H. Moradi. "Development of Inverse Receptance Coupling Method for Prediction of Milling Dynamics." In ASME 2010 10th Biennial Conference on Engineering Systems Design and Analysis. ASMEDC, 2010. http://dx.doi.org/10.1115/esda2010-24912.

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Receptance coupling substructure analysis (RCSA) is extensively used to determine the dynamic response of milling tool at its tip for the purpose of prediction of machining stability. A major challenge in using this approach is the proper modelling of the joint between the substructures and determination of its parameters. In this paper, an inverse RCSA is developed for experimental extraction of tool-holder frequency response function (FRF) including joint parameters. The accuracy and efficiency of this method is evaluated through an analytical investigation. It is shown that the extracted ho
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Duca, Radu-Corneliu, Matteo Creta, Katrien Poels, Lode Godderis, and Jeroen Vanoirbeek. "855 Dermal exposure to diisocyanates: development and validation of an analytical method for accurately assessment of very low levels of exposure." In 32nd Triennial Congress of the International Commission on Occupational Health (ICOH), Dublin, Ireland, 29th April to 4th May 2018. BMJ Publishing Group Ltd, 2018. http://dx.doi.org/10.1136/oemed-2018-icohabstracts.1185.

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Peral Moreno, Alonso, Francisco Javier Marquina Zárraga, Francisco José Prieto Santos, and Francisco Javier Gómez Sánchez. "Experimental Validation of a Non-Linear Buckling Method on a Rear Engine Mount Support Structure." In ASME Turbo Expo 2014: Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/gt2014-25114.

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Traditionally buckling analyses in engine structures have been performed using analytical solutions from validated bibliographical reference (e.g. Bruhn). This method requires a certain margin of safety due to the idealization of the real complex geometries into the more simple validated set of cases. As computational power increased, linear Euler buckling based on finite element solutions has become accessible. This second approach also requires of a certain margin of safety due to not considering material and geometrical non-linear effects. This paper presents the development of an accurate
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Reports on the topic "Analytical Method Development and Validation"

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Cetin, Ali, and Rainer Dahlmann. Recyclates for sustainable food contact method development for the validation of migration barriers. Universidad de los Andes, 2024. https://doi.org/10.51573/andes.pps39.ss.cep.3.

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Ideological changes in industrial approaches require greater ecological thinking. Regarding plastics, the integration of plastic waste into the circular economy arises from the urgent need to design and develop sustainable alternatives. The primary objective of a recycling process is to ensure that the quality of recycled plastics consistently matches that of the original product. Regional authorities and regulations require the assessment and prevention of the potential safety hazards of possible contaminants in recycling streams, recycling processes, and recycling technologies. The specific
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Scircle, Austin, Rebecca Crouch, Jared Smith, et al. Validation of sample extraction and analysis techniques for simultaneous determination of legacy and insensitive munitions (IM) constituents. Engineer Research and Development Center (U.S.), 2024. http://dx.doi.org/10.21079/11681/49412.

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Currently, no standardized method exists for the analysis of insensitive munitions (IM) in environmental matrices such as water, soils, and tis-sues. However, standardized methods, such as United States Environmental Protection Agency (EPA) 8330B, exist for legacy munitions for water and soil matrices. The lack of standardized methods for IM analysis leads researchers to use a wide variety of incomplete and overlapping analytical methodologies. The overall project’s first phase, Strategic Environmental Research and Development Program (SERDP) Environmental Restoration (ER)–2722, was to develop
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Fu. L51878 Methods for Assessing Corroded Pipeline-Review Validation and Recommendations. Pipeline Research Council International, Inc. (PRCI), 2002. http://dx.doi.org/10.55274/r0010358.

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An assessment of the remaining strength of corroded line pipe is generally accomplished using the ASME B31G method and RSTRENG methods. These methods were developed using an early fracture mechanics relationship for toughness-independent failure of pressurised pipes and were empirically calibrated against a database of around 80 full-scale burst tests for thin wall pipes, dominated by pipes of grade B and grade X52. Applications of these methods to modern higher toughness pipe materials have not been fully justified. Neither of these methods is able to assess the significance of interactions b
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Laber, Charles, Guilherme Lotufo, Austin Scircle, Jenifer Netchaev, and Anthony Bednar. Overview of microscale analytical methods for the quantitative detection of bioaccumulative contaminants in small tissue masses. Engineer Research and Development Center (U.S.), 2024. http://dx.doi.org/10.21079/11681/48190.

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Abstract:
For many bioaccumulation studies, generation of large sample masses of exposed organisms is challenging or even prohibitive. Therefore, the use of smaller sample masses for analysis without compromising data quality or quantitative level achieved is desirable. To this end, a variety of microanalytical procedures have been developed that used 1 g or less of tissue to address specific experimental challenges. However, these methods have not been systematically evaluated or published. The present work evaluates the current state of the microanalytical methods reported and identifies additional ne
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FENKER, KALEE. ANALYTICAL RADIOCHEMICAL METHOD DEVELOPMENT FOR MARK 18A PROGRAM. Office of Scientific and Technical Information (OSTI), 2023. http://dx.doi.org/10.2172/1958207.

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Dewberry, R. A. Development of total uranium analytical method by L x-ray fluorescence. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/491554.

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Woolf, Reagan K. Flight Test Validation of an Analytical Method for Predicting Trailing Cone System Drag Force and Droop Angle. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada583117.

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Eppich, G., J. Wimpenny, Q. Yin, and B. Esser. California GAMA Special Study: Stable isotopic composition of groundwater boron - analytical method development. Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1111133.

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Washington, Aaron L., William Narrows, Jonathan H. Christian, and Leroy Msgwood. Quantitative analysis of concrete using portable x-ray fluorescence: Method development and validation. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1373540.

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Susan S. Sorini and John F. Schabron. CHEMICAL SENSOR AND FIELD SCREENING TECHNOLOGY DEVELOPMENT: FUELS IN SOILS FIELD SCREENING METHOD VALIDATION. Office of Scientific and Technical Information (OSTI), 1997. http://dx.doi.org/10.2172/772384.

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