<p><strong>This leaflet is intended as a comprehensive checklist outlining the key steps to consider when participating in a proficiency testing (PT) scheme. Selection of an appropriate PT scheme must be ensured [1]. It provides essential tips to help participants avoid common mistakes and achieve successful outcomes. The main stages of PT participation are covered, from receipt of PT items through to the review of received evaluations [1-3]. Documentation of outcomes for many of the topics addressed below is recommended, particularly for accreditation purposes.&nbsp;</strong></p><h4><strong>1. Prior to PT participation&nbsp;</strong></h4><ul><li>Verify that the PT provider has up-to-date billing, shipping and technical contact information for the laboratory.&nbsp;</li><li>Ensure that the laboratory has documented procedures in place or, if necessary, prepare procedures for: reviewing PT results upon receipt; taking corrective actions when assessments indicate poor performance; conducting periodic reviews of PT results over time; storing PT reports.&nbsp;</li></ul><h4><strong>2. Receipt of PT items&nbsp;</strong></h4><ul><li>Open the package of PT items immediately upon receipt to check their condition. Contact the PT provider and request a replacement if any PT items are missing, broken, leaking or otherwise compromised.&nbsp;</li><li>Study the PT provider’s instructions carefully to ensure they are clear and understandable (e.g. handling, storage, pre-treatment, preparation, reporting of results).&nbsp;</li><li>Register, identify, and mark the PT items according to normal procedures in the laboratory.&nbsp;</li><li>Store the PT items in accordance with any instructions provided.&nbsp;</li></ul><h4><strong>3. Measurements&nbsp;</strong></h4><ul><li>Read the instructions supplied by the PT provider carefully before starting the measurements.&nbsp;</li><li>Carry out the measurements under conditions as close as possible to routine testing, unless otherwise instructed by the PT provider.&nbsp;</li><li>Ensure that the analysis is carried out to meet any measurement deadline requirements.</li></ul><h4><strong>4. Reporting results&nbsp;</strong></h4><ul><li>Allow sufficient time for reporting the results to the PT provider.&nbsp;</li><li>Report all the information required by the PT provider.&nbsp;</li><li>Ensure that the results are reported in the requested format (e.g. units, number of significant figures, decimal places).&nbsp;</li><li>Ensure that the results you are going to submit are those that you intend, correcting for any identified transcription errors (e.g. mix-up of samples or analytes).&nbsp;</li><li>Confirm that the submission process of the results to the PT provider has been completed.&nbsp;</li></ul><h4><strong>5. Reviewing PT reports&nbsp;</strong></h4><ul><li>Read the PT report as soon as possible and check that your results and other information are correctly represented; report any errors immediately to the PT provider.&nbsp;</li><li>Take notice of any comments on the specific PT round, evaluation of performance, and other matters relevant to the results of the PT round which provide valuable context to your individual results.&nbsp;</li><li>Review your assessed performance carefully in accordance with your laboratory procedures.&nbsp;</li><li>Store the PT report according to internal procedures.&nbsp;</li></ul><h4><strong>6. Follow-up on participation in a PT scheme&nbsp;</strong></h4><ul><li>Investigate any poor performance in accordance with your laboratory quality system [4].&nbsp;</li><li>Evaluate the impact of poor performance (e.g. risk that poor quality data may have been reported to customers).&nbsp;</li><li>Implement any corrective actions as relevant, and if possible, make use of any surplus PT items [5] to assess effectiveness.&nbsp;</li><li>Monitor any trends in performance over time, concentration levels, etc.&nbsp;</li></ul><blockquote><p>Information about PT providers and PT schemes can be obtained from your national accreditation body, from the <a target="_blank" rel="noopener noreferrer" href="https://www.eptis.org/"><strong>EPTIS website</strong></a> or from other national or international organizations.</p></blockquote>

Basic instructions for participants in a proficiency testing scheme

<p><strong>Our Library never stops expanding. What are the most recent contributions to LabRulezICPMS Library in the week of 9th March 2026? Check out new documents from the field of spectroscopy/spectrometry and related techniques!</strong></p><blockquote><p><span style="font-size:20px;">👉 </span><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library"><span style="font-size:20px;"><strong>SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT SPECTROSCOPY/SPECTROMETRY RELATED TECHNIQUES</strong></span></a></p></blockquote><blockquote><p><strong>👉 Need info about different analytical techniques?</strong> Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library"><strong>LabRulezLCMS</strong></a> or <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library"><strong>LabRulezGCMS</strong></a> libraries.</p></blockquote><p>This week we bring you application notes by <strong>Agilent Technologies</strong>, <strong>Metrohm,</strong> <strong>Shimadzu </strong>and<strong> Thermo Fisher Scientific!</strong></p><h3><strong>1. Agilent Technologies: Spectral Transmission Measurements of Pharmaceutical Packaging</strong></h3><p><strong>Using the </strong><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=Cary+60+UV%E2%80%91Vis"><strong>Agilent Cary 60 UV‑Vis</strong></a><strong> Diffuse Reflectance Accessory following EP &lt;3.2.1&gt;, USP &lt;660&gt;, and USP &lt;661.2&gt;</strong></p><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_pharmaceutical_packaging_transmission_cary_60_uv_vis_dra_5994_8889en_agilent_2c933e5576.pdf"><strong>Full PDF for download</strong></a></li></ul><p>Pharmaceutical containers play a significant role in maintaining final drug stability, integrity, and safety, from manufacturing to distribution to the end user. The ability of the packaging system to protect the drug from external agents is critical for quality assurance. Therefore, all pharmaceutical packaging systems must conform to stringent standards.&nbsp;</p><p>Plastic and glass are commonly used materials for packaging, and they are typically transparent or opaque. Transparency to ultraviolet (UV) light can pose a risk to light‑sensitive pharmaceuticals, as exposure can initiate adverse—and sometimes harmful—photochemical reactions that can significantly affect drug quality and reduce shelf-life.<sup>1</sup>&nbsp;</p><p>The EP and USP define well-established standards, designed to measure physiochemical and functional properties of packaging components intended to contain a drug product (pharmaceutical containers), to meet regulatory requirements. The EP Chapter &lt;3.2.1&gt; Glass Containers for Pharmaceutical Use includes a functionality test method to demonstrate adequate light resistance of colored glass containers through spectral transmission measurement. An included acceptance criterion specifies the allowed maximum amount of light transmitted by the tested material, defined by the drug product dosage administration form. For example, for glass containers that package oral drug products, the acceptance criterion defines that the observed spectral transmission should not exceed 10% at any wavelength in the range of 290 to 450 nm (&lt; 10%T).<sup>2</sup> The identical test and criterion are found in USP Chapter &lt;660&gt; Containers – Glass.<sup>3</sup> In addition, the USP Chapter &lt;661.2&gt; Plastic Packaging Systems for Pharmaceutical Use also includes the analogous functionality test method and acceptance criterion for plastic pharmaceutical packaging.<sup>4&nbsp;</sup></p><p>The <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=10&amp;search=Cary+60+UV%E2%80%91Vis"><strong>Cary 60 UV-Vis spectrophotometer</strong></a>, equipped with the Cary 60 UV-Vis DRA, was chosen for measurement due to its extended ability to reliably measure precise transmission of scattering materials (Figure 1). The Cary 60 UV-Vis is a versatile spectrophotometer; however, measuring materials like plastics and glass, which are textured, translucent, or opaque in a manner that scatters light can result in challenges in satisfactorily measuring light transmittance with standard techniques. In a standard spectrophotometer, scattering materials tend to diffuse transmitted light, deviating an unquantifiable amount of light from the direct optical path of the detector. The detector may not collect all the scattered (lost) light, resulting in inaccurate measurements and results.&nbsp;</p><p>For this reason, the Cary 60 UV-Vis was equipped with an internal DRA, which uses a 50 mm integrating PTFE-coated sphere that easily sits inside the spectrophotometer's sample compartment. For these applications, using a DRA can optimize light collection. The sphere's design captures all scattered light uniformly, overcoming scattering losses for accurate measurement of transmitted light. In applications where total transmission is crucial for quality assurance, the DRA is an essential tool for accurate measurements.</p><h4><strong>Conclusion&nbsp;</strong></h4><p>In this application note, an Agilent Cary 60 UV-Vis spectrophotometer, fitted with an Agilent Cary 60 UV‑Vis DRA, was used to reliably and quickly determine the spectral transmission of packaging systems used for pharmaceuticals, following the EP &lt;3.2.1&gt;, USP &lt;660&gt;, and USP &lt;661.2&gt; test methods for functionality of light-resistant packaging systems. The integrating sphere enabled the instrument to accurately measure total transmittance of plastic and glass (scattering) materials.&nbsp;</p><p>All containers presented less than the defined maximum %T specification, demonstrating light-resistance functionality for containing light-sensitive drug products for oral administration. This method illustrates the importance of accurate testing for quality assurance of pharmaceutical packaging. The Agilent Cary 60 UV-Vis spectrophotometer, paired with Cary WinUV Pharma software, delivers secure data management and compliance for regulated pharmaceutical labs.</p><h3><strong>2. Metrohm: Multiparameter hops analysis by near-infrared spectroscopy (NIRS)</strong></h3><p><strong>Rapid determination of alpha acids, beta acids, cohumulone content, total oil content, HSI, and moisture</strong></p><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_nir_130_download_6177b89ee1.pdf"><strong>Full PDF for download</strong></a></li></ul><p>The quality of hops and hop pellets is vital across the entire brewing supply chain. Traditional methods used for quality control (e.g., titration and HPLC) are highly accurate and widely accepted. They are also time consuming, labor intensive, and dependent on chemical reagents which not only incur ongoing material costs but also require careful handling and proper disposal. Near-infrared spectroscopy (NIRS) offers a compelling alternative when ultra-high precision is not necessary. It enables the rapid analysis of multiple parameters within a minute without using any chemicals. This Application Note outlines the measurement setup and the results of cohumulone, hop oils, and moisture content, the hop storage index (HSI), and hops acids analysis with NIRS.</p><h4><strong>EXPERIMENTAL EQUIPMENT&nbsp;</strong></h4><p>More than 500 fresh hop samples and ground hop pellets were analyzed on an <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=220&amp;search=omnis+nir"><strong>OMNIS NIR Analyzer Solid</strong></a> (Figure 1). The samples were added to an OMNIS sample cup and analyzed in diffuse reflection mode. To include sample variety, the sample rotated during measurement to collect spectra from different locations. The automatically averaged spectra were used for model development. Spectra acquisition, model development, and validation were carried out with the OMNIS Software.&nbsp;</p><p>Reference values for alpha acids were obtained using various official methods, including EBC 7.4, EBC 7.5, and EBC 7.7. Total oils and beta acid content were determined using EBC 7.4, while EBC 7.7 was employed for cohumulone analysis. Moisture content and the hop storage index (HSI) were measured using a halogen moisture analyzer and a UV-VIS photometer, respectively.</p><h4><strong>CONCLUSION</strong></h4><p>This Application Note demonstrates the feasibility of using NIR spectroscopy for the analysis of freshly harvested hops and ground hop pellets to determine cohumulone, moisture, and total oil content, HSI, and alpha and beta acids. Using alpha acids as an example, the difference between a prediction model covering the full concentration range and a model specific to a narrower range was highlighted. The latter reduced the prediction error by a factor of two.&nbsp;</p><p>Users can apply this approach to maximize accuracy. In the OMNIS Software, both models can be combined to automatically perform the following sequence. First, the alpha acid concentration is estimated using the broad-range model; then, a more precise prediction is made using the restricted-range model.</p><h3><strong>3. Shimadzu: Observation of Acrylic Block Fracture during Impact Compression Using the Hopkinson Bar Method</strong></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_01146_en_dc42e77a9c.pdf"><strong>Full PDF for download</strong></a></li></ul><h4><strong>User Benefits</strong></h4><ul><li>The HPV -X3 offers three times the resolution of conventional models, enabling observation of specimen fracture at much higher resolution.</li><li>With a maximum frame rate of 20 Mfps, the HPV-X3 is well-suited for observing high-speed phenomena such as an impact test</li></ul><p>Understanding materials properties is critical to product design. In particular, for applications such as transportation equipment, where materials may be subjected to impact loads, it is essential to evaluate not only static properties but also impact properties. When subjected to impact, materials may exhibit stress and strain characteristics different from those under static loading, making it essential to quantify these characteristics through impact testing.&nbsp;</p><p>The Hopkinson bar method is a well-established technique for impact compression testing. Proposed by B. Hopkinson, this method enables detailed analysis of a material’s impact response and evaluation of its fracture properties by subjecting the specimen to a sudden force using a bar-launching device. This paper presents an example of an impact compression test on an acrylic specimen with a central circular hole, recorded with an HPV-X3 high-speed video camera (Fig. 2) using the Hopkinson bar method.</p><h4><strong>Imaging System&nbsp;</strong></h4><p>The imaging devices are listed in Table 1, and the imaging conditions are listed in Table 2. As shown in Fig. 4(b), laser illumination was directed from the rear of the specimen toward the lens, and imaging was performed with the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=HPV-X3"><strong>HPV-X3</strong></a> using a close-up ring, bellows, and macro lens. This setup enabled observation of the fracture process in the acrylic block. Two types of imaging were conducted: observation of crack propagation immediately after loading, and observation of subsequent fracture.</p><h4><strong>Conclusion&nbsp;</strong></h4><p>The impact compression test of an acrylic specimen using the Hopkinson bar method was observed using the HPV-X3 highspeed video camera. Inside the compressed specimen, the propagation of a wavefront believed to be a stress wave was first observed. Subsequently, cracks propagated from the central circular hole toward the left and right surfaces, and finally, diagonal cracks formed, leading to complete fracture. The progress of this series of fracture processes was clearly captured.&nbsp;</p><p>The HPV-X3 has three times the resolution of the previous <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=HPV-X2"><strong>HPVX2 model</strong></a>, enabling more detailed observation of specimens during impact tests, including the Hopkinson bar method. Furthermore, because fracture phenomena during impact testing occur at high speeds, the HPV-X3, which can record images at up to 20 Mfps, is ideal for capturing them.</p><h3><strong>4. Thermo Fisher Scientific: Analysis of silica in air filters using ARL X’TRA Companion X-ray Diffractometer</strong></h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/analysis_of_silica_in_air_an41521_a3b8eb33d5.pdf"><strong>Full PDF for download</strong></a></li></ul><p>The analysis of silica in air filters is a critical aspect of occupational health and safety, aimed at protecting workers from the harmful effects of inhaling crystalline silica particles, which can lead to diseases such as silicosis and lung cancer. The NIOSH 7500 method (NIOSH, 2003) provides a detailed and standardized procedure for the determination of crystalline silica in air samples using X-ray diffraction (XRD). This method involves the collection of air samples on filters, which are then analyzed to identify and quantify the crystalline silica phases, including quartz, cristobalite, and tridymite.&nbsp;</p><p>XRD is chosen for its high specificity and sensitivity in distinguishing different crystalline forms of silica, making it a reliable analytical technique. The method outlined in NIOSH 7500 requires meticulous sample preparation, including the proper collection and handling of air filters, calibration with known standards, and strict adherence to analytical parameters to ensure accurate and reproducible results. Following the NIOSH 7500 norm and equivalent standards helps ensure the reliable monitoring of workplace air quality, thereby safeguarding workers’ health. The use of XRD in analyzing silica in air filters is an essential component of industrial hygiene and environmental monitoring programs, facilitating the detection and control of hazardous silica exposure in occupational settings.</p><h4><strong>Instrument and software&nbsp;</strong></h4><p>The <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2296"><strong>Thermo Scientific™ ARL™ X’TRA Companion X-ray Diffractometer</strong></a> (c.f. Figure 1) is a simple, easy-to-use benchtop XRD instrument for routine phase analysis as well as more advanced applications. The ARL X’TRA Companion XRD uses a θ/θ goniometer (160 mm radius) in Bragg-Brentano geometry coupled with a 600 W X-ray source (Cu or Co). The radial and axial collimation of the beam is controlled by divergence and Soller slits, while air scattering is reduced by a variable beam knife. An integrated water chiller is available on demand. Thanks to the innovative solid state pixel detector (55 x 55 μm pitch), the ARL X’TRA Companion XRD provides very fast data collection and comes with one-click Rietveld quantification capabilities and automated result transmission to a LIMS (laboratory information management system).</p><h4><strong>Your benefits&nbsp;</strong></h4><p>The ARL X’TRA Companion XRD provides data perfectly suited to quantify respirable quartz in air filters. Utilizing a calibration curve in a one-click refinement delivers results within minutes, ensuring ease-of-use for operators and reducing training requirements. XRD analysis of air filter samples complies with the NIOSH 7500 standard.</p>

News from LabRulezICPMS Library - Week 11, 2026

<p><strong>How can we make the production of supercapacitors for energy storage more sustainable and replace the traditionally used but toxic solvent NMP (N-methyl-2-pyrrolidone)? According to scientists from CATRIN at Palacký University, the “green” solvents Cyrene and Tamisolve may be a suitable alternative. In an article published in the </strong><a target="_blank" rel="noopener noreferrer" href="https://www.sciencedirect.com/science/article/pii/S1385894725130696?via%3Dihub#s0060"><i><strong>Chemical Engineering Journal</strong></i></a><strong>, they have shown that these solvents can be used in production without reducing the performance of the equipment. They thus offer a path to the next generation of sustainable, high-performance supercapacitors for industrial use.</strong></p><p>“<i>Supercapacitors are one of the modern technologies for storing electric energy. As sustainable energy storage becomes more prominent, it is essential to replace the hazardous solvents used in the production of supercapacitor electrodes. Our study presents Cyrene and Tamisolve as environmentally friendly alternatives to the toxic solvent NMP, which is traditionally used in production. Both tested solvents enabled the preparation of electrodes that maintain high electrochemical performance while improving environmental compatibility</i>,” said <strong>Michal Otyepka</strong>, <strong>corresponding author</strong> of the article.</p><p>The electrodes were prepared using nitrogen-doped graphene as the active material in combination with two types of binders. The first was a common fluorinated binder (PVDF), which is widely used in industry, including in the manufacturing of battery electrodes. The researchers also tested a fluorine-free binder (PVP), which has a lower environmental impact and is more soluble in environmentally friendly solvents. Using various combinations, they monitored the performance and stability of the electrodes as well as their mechanical resistance.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/CATRIN_Vedci_z_CATRIN_nabizeji_zelenejsi_cestu_pro_vyrobu_superkondenzatoru_443775296a.jpg" alt="CATRIN: CATRIN researchers offer a “greener” way to make supercapacitors" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_CATRIN_Vedci_z_CATRIN_nabizeji_zelenejsi_cestu_pro_vyrobu_superkondenzatoru_443775296a.jpg 245w," sizes="100vw" width="1536" height="768"></p><p>“<i>The results showed that not only can the alternative solvents Cyrene and Tamisolve fully replace the toxic solvent NMP, but also that the prepared electrodes have the necessary mechanical properties. Their compatibility with both fluorinated PVDF and non-fluorinated PVP binders, together with excellent layer uniformity and electrochemical stability, makes them ideal for use in scalable applications. This is essential for industrial production,</i>” said the publication’s <strong>first author, Ivan Dědek</strong>.</p><p>Cyrene, or dihydrolevoglucosenone, is obtained from renewable biomass sources such as cellulose. Tamisolve (N-butyl-2-pyrrolidone) is a substance related to the commonly used NMP, but is more gentle on human health and the environment.</p><p>Supercapacitor research has been a priority at CATRIN for almost ten years. In addition to developing new active materials, such as the successful nitrogen-doped graphene (SC-GN3), it also focuses on environmentally friendly and industrially feasible manufacturing processes. The replacement of toxic NMP with the “greener” solvents Cyrene and Tamisolve confirms that more sustainable production can go hand in hand with high performance and represents an important step towards industrial implementation.</p><blockquote><h4><strong>The original article</strong></h4><h4><a target="_blank" rel="noopener noreferrer" href="https://www.sciencedirect.com/science/article/pii/S1385894725130696?via%3Dihub#s0060"><strong>Toward transitioning to green and sustainable supercapacitors</strong></a></h4><p>Ivan Dědek, Vojtěch Kupka, Veronika Šedajová, Petr Jakubec, Matěj Navrátil, Michal Otyepka&nbsp;</p><p>Chemical Engineering Journal, 529, 2026, 172220</p><p><a target="_blank" rel="noopener noreferrer" href="https://doi.org/10.1016/j.cej.2025.172220">https://doi.org/10.1016/j.cej.2025.172220</a></p><h6>licensed under <a target="_blank" rel="noopener noreferrer" href="https://creativecommons.org/licenses/by/4.0/"><strong>CC-BY 4.0</strong></a></h6></blockquote><h4><strong>Abstract</strong></h4><p>The rapid advancement of supercapacitor technologies has intensified the demand for sustainable electrode fabrication methods that minimize environmental impact. A major challenge arises from the extensive use of the toxic solvent N-methyl-2-pyrrolidone (NMP), which is subject to increasingly stringent regulatory restrictions. We demonstrate that NMP can be effectively replaced with two green solvents, dihydrolevoglucosenone (Cyrene) and N-butyl-2-pyrrolidone (Tamisolve), without compromising electrochemical performance. Electrode formulations were prepared using nitrogen-doped graphene as the active material, in combination with either polyvinylidene fluoride (PVDF), a widely employed fluorinated binder, or polyvinylpyrrolidone (PVP), a non-fluorinated alternative with improved environmental profile. Optimized coatings exhibited high mass loadings exceeding 6 mg cm−2 while maintaining strong adhesion to current collectors, an often overlooked yet critical parameter for scalable manufacturing. Electrochemical testing revealed that PVDF in Cyrene delivered an energy density of 66.6 Wh kg−1 at a power density of 1.85 kW kg−1, with excellent cycling stability, retaining 91 % of capacitance after 100,000 cycles. PVP in Cyrene provided a more environmentally benign alternative, achieving an energy density of 64.2 Wh kg−1 at 1.80 kW kg−1, with 78 % capacitance retention after 100,000 cycles, thereby highlighting the trade-off between performance and sustainability.</p>

CATRIN researchers offer a “greener” way to make supercapacitors

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Eurachem is a European network promoting international traceability of chemical measurements and good analytical practice. It provides expert guidance, supports method validation, uncertainty evaluation, proficiency testing, and facilitates discussion on technical and policy issues in analytical quality.

Eurachem

The Czech Advanced Technology and Research Institute (CATRIN) at Palacký University is a cutting-edge scientific hub dedicated to advancing research in the fields of nanotechnology, biotechnology, and biomedicine. At its core, CATRIN boasts outstanding scientific teams, featuring international researchers. We emphasize interdisciplinarity, foster global collaborations, and work to translate our research findings into practical applications.

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Thermo Scientific Qtegra Intelligent Scientific Data Solution Software

The Thermo Scientific™ Qtegra™ Intelligent Scientific Data Solution (ISDS) Software is a software platform built on four pillars.

<p><strong>The Thermo Scientific™ Qtegra™ Intelligent Scientific Data Solution (ISDS) Software is a software platform built on four pillars, designed to deliver a complete solution for laboratories depending on productivity, scalability, and quality results to achieve their goals.</strong></p><h5><strong>Intelligent</strong></h5><p>Built-in intelligence facilitates the <strong>full workflow from sample to results</strong>. Laboratories can be <strong>more reactive and profitable</strong>, with software that facilitates data driven decisions more efficiently.</p><h5><strong>Scientific</strong></h5><p>Developed with scientific integrity, Qtegra ISDS Software delivers high quality, reliable <strong>data that labs can trust</strong>. Data transparency lets laboratory personnel focus on other tasks while ensuring the utmost confidence in scientific collaboration.</p><h5><strong>Data</strong></h5><p>Data is the key to success for all laboratories. Qtegra ISDS Software can help labs excel at efficiently <strong>delivering consistent and relevant results</strong> with extensive tools to effectively acquire and manage data.</p><h5><strong>Solution</strong></h5><p>Laboratories can enjoy the familiarity of common <strong>software across multiple analytical systems</strong> while differentiating their offering through customizable and application specific workflows.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_2_78dbb0f7f5.jpg" alt="Thermo Fisher Scientific: Thermo Scientific Qtegra Intelligent Scientific Data Solution Software" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_2_78dbb0f7f5.jpg 217w," sizes="100vw" width="1535" height="1101"></p><h4><strong>Routine analysis</strong></h4><p>High-throughput production and contract testing laboratories benefit from the assistance and economy imparted through <strong>Qtegra ISDS Software</strong>. The design facilitates integration in a growing lab ecosystem, while <strong>intuitive workflow features</strong>, <strong>interference management </strong>and <strong>pertinent data visualization</strong> lets laboratories acquire and interpret data confidently, quickly, and with ease. Laboratories performing routine testing can ensure profitability through productivity, quality data, and right first-time analysis.</p><h4><strong>Scientific research</strong></h4><p>Researchers looking to push the boundaries of innovation in their field can focus intently on science, confident in the knowledge that Qtegra ISDS Software provides <strong>flexibility of customized configurations with multiple acquisition modes</strong> and <strong>data processing tools</strong> to probe and access new data. Within a framework that is exceptionally easy to set up and switch between configurations, Qtegra ISDS Software enables research labs with multiple users to focus on the data rather than the analysis.</p><h4><strong>Regulated industries</strong></h4><p><strong>Food, environmental and pharmaceutical QA/QC </strong>are amongst the sectors that are constantly being challenged to meet rising standards of quality and to comply with rigorous regulatory requirements, whether they be analytical or procedural. Qtegra ISDS Software recognizes these challenges and includes the necessary tools for laboratories to rapidly meet their compliance goals.</p><h4><strong>Integrated lab assistant saves time, simplifies sample preparation, and intelligently assists data analysis.</strong></h4><ul><li>Lab is <strong>quickly alerted to QC anomalies</strong> and samples above Maximum Allowable Concentrations.</li><li>Integrated, flexible <strong>QA/QC protocols</strong> minimize failures and prevent costly re-runs.</li><li>Intuitive <strong>color-coding of data and reports</strong> aids faster interpretation and decision making.</li><li><strong>Calculations</strong> are transparently applied in real time and can be audited easily.</li><li><strong>Prescriptive sample dilutions</strong> save labor and mitigate errors.</li><li><strong>Intelligent uptake and rinses</strong> optimize throughput and limit carryover challenges.</li><li>Intelligent <strong>over-range autodilution of high concentration samples</strong> automatically generates usable data without user input or delays</li></ul><h4><strong>It’s not just about finding answers, it’s about finding the right answers</strong></h4><p>Qtegra ISDS Software helps labs <strong>achieve consistently accurate results</strong> through Interference Management. Many analytical techniques are prone to interferences that are difficult to remove. Qtegra ISDS Software can help <strong>identify and automatically mitigate interferences</strong><br>with full visibility.</p><p><strong>The Reaction Finder method development assistant for Thermo Scientific™ TQ-ICP-MS analyzers</strong> intelligently selects the optimal measurement mode settings based on method analytes, removing the complexity from TQ technology and dramatically decreasing method development time.</p><p><strong>Interelement correction (IEC) for the Thermo Scientific™ iCAP™ PRO Series ICP-OES</strong> provides the ability to correct for interferences based on intensity or concentration and conform with regulatory methods, such as EPA Method 200.7.</p><h4><strong>Gain deeper insights and accelerate innovation with the flexibility of different data evaluation modes and specific workflows.</strong></h4><h4><strong>IRMS Chromatogram</strong></h4><p>Enjoy simple and reliable <strong>compound-specific IRMS or trace elemental speciation</strong> with a fully integrated workflow including chromatographic device control and dedicated chromatographic data processing.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_IRMS_Chromatogram_7b0a3b5376.jpg" alt="Thermo Fisher Scientific: Thermo Scientific Qtegra Intelligent Scientific Data Solution Software - IRMS Chromatogram" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_IRMS_Chromatogram_7b0a3b5376.jpg 245w," sizes="100vw" width="615" height="331"></p><h4><strong>Laser ablation</strong></h4><p>Expand capabilities in spatial and depth characterization with solutions to <strong>integrate laser ablation systems</strong> and <strong>split-flow analysis</strong> with third-party plug-ins and laser ablation specific data evaluation.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_Laser_ablation_63e97c2a0a.jpg" alt="Thermo Fisher Scientific: Thermo Scientific Qtegra Intelligent Scientific Data Solution Software - Laser ablation" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_Laser_ablation_63e97c2a0a.jpg 245w," sizes="100vw" width="613" height="338"></p><h4><strong>Single particle</strong></h4><p>Explore the expanding fields of <strong>single cell and nanoparticle analysis</strong> with automated workflows and dedicated sample handling packages.</p><p><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_Single_particle_72be4bfa52.jpg" alt="Thermo Fisher Scientific: Thermo Scientific Qtegra Intelligent Scientific Data Solution Software - Single particle" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Thermo_Fisher_Scientific_Thermo_Scientific_Qtegra_Intelligent_Scientific_Data_Solution_Software_Single_particle_72be4bfa52.jpg 245w," sizes="100vw" width="615" height="329"></p><h4><strong>How do you manage large volumes of data in your laboratory?</strong></h4><p>Leverage data management and flexible and intuitive data processing tools within Qtegra ISDS Software to excel at delivering consistent data on time.</p><h5><strong>Data security</strong></h5><p>Be confident with the knowledge that <strong>all data is secure and encrypted, yet easily accessible</strong>. The Qtegra ISDS Software LabBook concept ensures the whole analytical workflow from samples to results is stored in one secure container.</p><h5><strong>LIMS integration</strong></h5><p>Complete analysis descriptions can be <strong>directly imported into Qtegra ISDS Software</strong>, eliminating additional user input. Full results, both analytical and metadata, are immediately available after analysis for rapid turnaround of results.</p><h5><strong>Data visualization</strong></h5><p>Access relevant data quickly, with flexibility to dig deeper when needed, enabling quicker decisions and efficiency.</p><h5><strong>Enhanced LabBook query</strong></h5><p>Combine data across <strong>LabBooks</strong> for method validation, long-term performance, or finding relationships and gaining deeper insights into data.</p><h5><strong>Flexible data export</strong></h5><p>Export data <strong>in the format you need</strong> for archiving, reporting, or further data processing and interrogation.</p><h5><strong>Comprehensive data reporting</strong></h5><p><strong>Automated report generation</strong> makes data management effortless. <strong>Customize report formats</strong> to fit with the needs of your customers.</p><h5><strong>Data management</strong></h5><p><strong>Store and manage data</strong> effortlessly with an intuitive file browser.</p><h5><strong>User management</strong></h5><p>Control access for <strong>up to 5 user levels </strong>with comprehensive user management.</p>

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