<h4>Types of comparisons&nbsp;</h4>Interlaboratory comparisons mean organisation, performance and evaluation of measurements and tests on the same or similar items by two or more laboratories in accordance with predetermined conditions. Comparisons are organised at all scientific levels, but the objectives, protocols and participants vary. In certification trials, the measurements are used to assign values to reference materials. In method validation studies (collaborative trials), the performance, e.g. trueness and precision of methods, is evaluated. The most accurate measurements are compared world-wide in ’key comparisons’.&nbsp;Proficiency testing (PT) schemes – also known as ‘external quality assessment (EQA) schemes’ or ‘laboratory performance studies’ – are one means of assessing the quality of routine measurements. PT schemes are the most common, and perhaps the most important, type of interlaboratory comparisons.&nbsp;<h4>Advantages of PT&nbsp;</h4>Participation in PT enables you to compare your results with those from other laboratories. It can also provide you with:&nbsp;<ul><li>Regular, objective and independent assessment of the quality of your routine analyses;&nbsp;</li><li>Feedback that stimulates improvement of the technical work;</li><li>Comparative information about method and instrument performance;</li><li>An overview of the quality of specific analyses in a sector, country or region.&nbsp;</li></ul><h4>Limitations of PT&nbsp;</h4>Ideally, PT samples are similar in nature to routine samples, and sufficiently homogeneous and stable not to influence the evaluation of participants’ performance. Due to practical aspects, PT samples are sometimes processed, e.g. stabilised and/or freeze-dried. Participants should be aware of this.&nbsp;PT schemes can be organised and evaluated in many different ways. There is no perfect protocol! For laboratories and their customers, and for accreditation and regulatory bodies, it can be important to know if the same result is judged differently by different PT providers.<h4>Appropriate PT schemes&nbsp;</h4>The huge number of analytes, and the large variety in the way tests are performed, means that it is not always possible to find a scheme that meets a laboratory’s exact requirements. Before signing up for a scheme, carefully check that the test materials, and the analytes and their levels fit your routine measurement procedures. Is the frequency appropriate and does the provider’s report give you sufficient information?&nbsp;<h4>Role of PT in measurement quality&nbsp;</h4>Correct measurements require both internal and external ‘tools’. During the validation step, the performance of the method is established. Subsequent use of control charts will show if the measurements are under statistical control. Many laboratories choose to accredit their services, thereby agreeing to implement a quality management system and accepting regular external audits of their work. Participating in PT is an effective external means to check that the procedures are fit for purpose!&nbsp;<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/Eurachem_Proficiency_testing_schemes_and_other_interlaboratory_comparisons_2_7688414cd9.jpg" alt="Eurachem: Proficiency testing schemes and other interlaboratory comparisons" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_Eurachem_Proficiency_testing_schemes_and_other_interlaboratory_comparisons_2_7688414cd9.jpg 206w," sizes="100vw" width="848" height="642"><h4>Educational aspects&nbsp;</h4>PT offers opportunities for education and training. Many providers have regular user meetings to discuss results and problem areas. Virtual PT schemes, using digital images of the samples, enable an unlimited number of participants, immediate feedback and repeated assessments.<h4>Accreditation of PT providers&nbsp;</h4>Some providers choose to accredit their PT schemes. The work with organising and evaluating the results will then be assessed according to international guidelines, similar to calibration and testing laboratories.<h4>Use of PT results&nbsp;</h4>Because PT schemes provide an overview of the analytical quality for specific applications, the results are increasingly used by laboratories’ customers, and by accreditation and regulatory bodies. PT helps identify measurement problems, which have a direct impact on trade, environmental monitoring, and health and safety.&nbsp;<h4>More information / further reading&nbsp;</h4>Information about PT providers and schemes can be obtained from your national accreditation body, from the <a target="_blank" rel="noopener noreferrer" href="https://www.eptis.org/">EPTIS website</a> or from other national or international organisations.

Proficiency testing schemes and other interlaboratory comparisons

We are excited to announce that registration for the 12th International Symposium on Recent Advances in Food Analysis (RAFA 2026), along with the call for abstracts and travel grants for young scientists, is now officially open!<h3>Key dates</h3><ul><li>May 31, 2026: Application for Young scientist travel grant</li><li>June 30, 2026<ul><li>Application for participation as a Sponsor or Exhibitor or Media partner</li><li>Abstract submission for oral presentation</li><li>Reduced registration fee</li></ul></li><li>August 31, 2026: Abstract submission for poster presentation</li><li>September 30, 2026: Last minute posters submission</li><li>November 3 - 6, 20026: 12th International Symposium on Recent Advances in Food Analysis (RAFA 2026) in Prague, Czech Republic</li></ul><h3>Registration</h3><blockquote>👉<a target="_blank" rel="noopener noreferrer" href="https://rafa.easyevent.eu/tickets/">Registration for RAFA 2026 is OPEN!</a>Early-bird registration until 30 June, 2026</blockquote>After successful submission of your registration, you will receive by e-mail (i) an automatic confirmation of receipt indicating the total amount of payment due (either for bank transfer or for on-line payment by card), (ii) login to Member section where you can administrate your profile, submit your abstracts, and from September 2026 register for satellite events, workshops and seminars. If it will not be delivered within a few minutes after submission of your registration please contact us at RAFA2026@vscht.cz.As soon as payment of registration fee is processed, you will also receive by e-mail (iii) confirmation of payment.<h4>Important notice:</h4>Registration fee of those who have submitted an abstract for oral or poster presentation has to be received until September 30, 2026, otherwise these contribution(s) will not be included into the Book of Abstracts and the Conference programme.<h4>Registration Fees</h4><ul><li>Smart rate (Until 30 June, 2026): € 655</li><li>Regular registration (Until 30 September, 2026): € 855</li><li>Late registration (From 1 October, 2026): € 955</li><li>Student rate*&nbsp;<ul><li>Until 30 June, 2026: € 465</li><li>From 1 July, 2026: € 605</li></ul></li></ul>* The proof of student status (e.g. copy of a student identify card) is requested as an attachment of the registration form.<h5>The regular registration fee will include:</h5><ul><li>Attendance at all scientific sessions, workshops, seminars, vendor seminars and other satellite events</li><li>Access to the poster and exhibition area</li><li>Conference kit (name badge, conference bag, conference documents, certificate of participation, certificate of presentation on request)</li><li>Final programme</li><li>E-Book of Abstracts</li><li>Coffee breaks</li><li>Buffet luncheons</li><li>Welcome drink</li></ul>In the registration form you can register free of charge for the welcome drink and you can also order ticket(s) for the conference dinner (€ 85).Please note that your registration is firm when your payment has been received.<h3>Abstract submission</h3><blockquote>👉<a target="_blank" rel="noopener noreferrer" href="https://rafa.easyevent.eu/tickets/">CALL for ABSTRACTS is OPEN!</a>In order to submit an abstract, you must first register to attend RAFA 2026. After registration you will receive an access to the Member section where you can submit your abstract(s).</blockquote>&nbsp;After successful submission of your abstract you will receive an automatic confirmation of receipt of submitted abstract via e-mail. If it will not be delivered within a few minutes after submission of your abstract please check at first your spam box-mail and then contact us at RAFA2026@vscht.cz.Please ensure that your abstract does not contain spelling, grammatical or scientific errors. Even though modifications of your submitted abstract will be allowed in the Abstract section of the Member section until the deadline for the abstract submission, please be confident on the lack of errors in your final version prior to starting the submission process.The abstract will be reproduced exactly as submitted. No proofreading will be done, although some corrections may be requested by the reviewers.If you need to withdraw your abstract, a written statement reflecting the reasons for this decision must be sent to RAFA2026@vscht.cz no later than September 30, 2026.<h4>Important notice:</h4><blockquote>1 registered participant can submit no more than 2 abstracts.</blockquote>To apply for a young scientist’s oral presentation, as an indication please respect the rule that you should be born in 1991 or later.The text of the abstract should be limited to 3000 characters including spaces. Tables and pictures are not allowed.Abstracts of oral presentations and posters will be included into the "e-Book of Abstracts" only after receipt of the conference registration fee. Any payment of the registration fee has to be received until September 30, 2026, otherwise contribution(s) will not be included into the e-Book of Abstracts and the Conference programme.<h3>Special opportunities for young scientists:</h3><ul><li>Dedicated slots for oral presentations within the main scientific programme</li><li>Competitive travel grants for young scientists</li><li>Award(s) for the best poster presentation(s)</li></ul>Whether you are a PhD student or an early-career researcher, RAFA 2026 offers a unique opportunity to present your work, gain international exposure and connect with leading experts in the field.Be part of this inspiring scientific event and join us in Prague!

RAFA 2026 - Registration & Call for Abstracts are now OPEN

Our Library never stops expanding. What are the most recent contributions to LabRulezICPMS Library in the week of 13th April 2026? Check out new documents from the field of spectroscopy/spectrometry and related techniques!<blockquote>👉 <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library">SEARCH THE LARGEST REPOSITORY OF DOCUMENTS ABOUT SPECTROSCOPY/SPECTROMETRY RELATED TECHNIQUES</a></blockquote><blockquote>👉 Need info about different analytical techniques? Peek into <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/library">LabRulezLCMS</a> or <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library">LabRulezGCMS</a> libraries.</blockquote>This week we bring you application notes by Metrohm, Shimadzu and Waters Corporation and other document byThermo Fisher Scientific!<h3>1. Metrohm: Dried pet food analysis by nearinfrared spectroscopy (NIRS)</h3>Rapid determination of moisture, protein, fat, and ash<ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_nir_129_download_9ff310dbb5.pdf">Full PDF for download</a></li></ul>Pet food testing involves accurate monitoring and control of moisture, protein, fat, and ash content. This allows pet food manufacturers to satisfy nutritional adequacy requirements, meet regulatory guidelines, and provide high-quality foods to pet owners. Traditional analysis methods are often slow and laborintensive. Near-infrared (NIR) spectroscopy provides a fast, nondestructive alternative for analyzing these key quality control parameters with minimal sample preparation. This study evaluates the use of NIR spectroscopy in the pet food industry for efficient and reliable quality control during dried pet food production.<h4>EXPERIMENTAL EQUIPMENT&nbsp;</h4>199 dried pet food samples (mainly dog and cat food) from different suppliers were analyzed in whole and ground forms on an <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=220&amp;search=OMNIS+NIR">OMNIS NIR Analyzer</a> Solid (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. Reference values were obtained by official methods such as ISO 6496 (moisture), ISO 5983 (protein), ISO 5984 (ash), and ISO 6492 (fat).<h4>CONCLUSION</h4>This Application Note demonstrates the feasibility of using NIR spectroscopy for the analysis of several pet food quality parameters, including protein, moisture, fat, and ash. Results indicate that lower prediction errors can be obtained when grinding pet food samples before their analysis. A comparison between different methods used for the analysis of pet food clearly highlights the significant time-saving potential of NIR spectroscopy (Table 1). Furthermore, the simplicity of the analysis and the availability of a pre-calibrated instrument, using the pre-calibration, dry pet food, solid (6.06008.027), make both the implementation and the application of NIR spectroscopy with OMNIS NIRS straightforward.<h3>2. Shimadzu: Determination of Elemental Impurities in Bioethanol Using ICP-MS</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/an_01_01021_en_942f8087b2.pdf">Full PDF for download</a></li></ul><h4>User Benefits</h4><ul><li>Bioethanol samples can be directly injected into ICP-MS for analysis.</li><li>Trace elements can be accurately determined with high sensitivity.</li></ul>To achieve carbon neutrality, bioethanol is expected to be one of the alternative energy sources to fossil fuels. First-generation bioethanol, produced mainly from corn, sugarcane, and similar crops, has been widely used. However, to avoid competition with food supplies, research and development are also advancing on second-generation bioethanol produced from non-food raw materials such as cellulosic materials. For example in Japan, seven companies including Toyota Motor Corporation have formed the raBit (Research Association of Biomass Innovation for Next Generation Automobile Fuels) to advance technologies for next-generation bioethanol. Shimadzu is also participating as a supporting member to promote R&amp;D through technical cooperation for analysis.&nbsp;Fuels in which bioethanol is blended into gasoline are referred to as E5 (up to 5% bioethanol), E10 (up to 10% bioethanol), etc.; using these fuels in vehicles can reduce environmental impact. At the same time, ethanol blended into gasoline and used as a fuel is required to meet trace element concentration limits (e.g., for copper) specified in standards such as ASTM D48061) and EN 153762). ICP-OES is commonly used for these analyses, but when ultra-trace impurity levels must be measured, higher-sensitivity ICP-MS is more suitable.&nbsp;In this Application, trace elements in first-generation and second-generation bioethanol were determined using the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=1&amp;search=ICPMS-2050">ICPMS-2050</a> (Fig. 1). Spike recoveries were also evaluated to confirm the validity of the analytical results.<h4>Conclusion</h4>In this Application, bioethanol was introduced directly into the ICPMS-2050 using an organic solvent introduction system to determine trace elements. Good spike recoveries were obtained, demonstrating that bioethanol can be analyzed accurately by direct injection.<h3>3. Thermo Fisher Scientific: <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2364">Thermo Scientific™ Nicolet™ FTIR</a> and <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2239">Thermo Scientific™ DXR Raman Microscope</a> Solutions</h3><ul><li>Other document</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/FL_52919_microspectroscopy_portfolio_flyer_516ee05816.pdf">Full PDF for download</a></li></ul>Microspectroscopy has become an essential tool in modern analytical laboratories, enabling detailed chemical identification and spatial analysis at the microscale. Whether working in pharmaceuticals, materials science, forensics, or electronics, selecting the right combination of FTIR or Raman microscopy is critical for achieving accurate and efficient results.Thermo Scientific offers a comprehensive portfolio of FTIR and Raman microscope solutions designed to match different analytical needs, user expertise levels, and throughput requirements. From routine QA/QC to advanced research applications, these systems provide scalable solutions for a wide range of analytical challenges .<h4>Matching the Right Tool to Your Application</h4>The portfolio is structured to help users “find their best fit” based on analytical complexity, required spatial resolution, and workflow demands. Entry-level configurations, such as the SurveyIR™ microspectroscopy accessory combined with Nicolet FTIR spectrometers, are ideal for routine identification tasks in QA/QC environments.As analytical needs increase, systems such as the Nicolet iN5 IR microscope with <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2364">Nicolet iS20 FTIR</a> offer improved spatial resolution and flexibility for more frequent analyses. These solutions are particularly suitable for laboratories performing regular identification of materials with moderate complexity.For advanced analytical workflows, integrated systems like the Nicolet iN10 IR microscope or Nicolet RaptIR+™ FTIR microscope provide enhanced capabilities, including spatial distribution analysis and high-resolution measurements down to the micrometer scale. These systems are designed for analytical service labs and R&amp;D environments where both identification and morphological insights are required.<h4>Expanding Capabilities with Raman Microscopy</h4>Raman microscopy complements FTIR by enabling high-resolution chemical imaging and analysis of complex samples. Systems such as the <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2239">DXR3 Raman microscope</a> and <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/2237">DXR3xi Raman imaging microscope</a> extend analytical capabilities to submicron spatial resolution, making them ideal for advanced research applications.These instruments allow users to not only identify compounds but also visualize their spatial distribution and morphology within a sample. This is particularly valuable in fields such as nanomaterials, semiconductors, and life sciences, where detailed structural and compositional information is required.<h4>From Identification to Imaging</h4>One of the key differentiators across the portfolio is the ability to move from simple identification to comprehensive imaging:<ul><li>Single-point analysis is available across all systems for rapid material identification</li><li>Small-area analysis enables localized chemical characterization</li><li>Large-area and spatial mapping provide insights into distribution and heterogeneity</li></ul>Higher-end systems, such as imaging microscopes, combine these capabilities with advanced automation and data processing tools, allowing users to efficiently analyze complex samples and extract meaningful insights .<h3>4. Waters Corporation: Accurate Particles Characterization in Lipid Nanoparticle Therapies</h3><ul><li>Application note</li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/labrulez-bucket-strapi-h3hsga3/720009097_en_15af008f22.pdf">Full PDF for download</a></li></ul>Lipid nanoparticles (LNPs) have emerged as one of the most promising drug delivery methods1. LNPs encapsulate genetic material in submicrometer sized lipid vesicles, deliver large biologic payloads, exhibit low immunogenicity, and can enable large manufacturing scalability as seen with the Moderna® and Pfizer® mRNA COVID-19 vaccines. Like all biologics, LNPs can be physically unstable2, aggregate, and form subvisible particles (SVPs), and thus need to be properly formulated and evaluated for physical and chemical stability3. The next generation of LNPs are even more chemically and biologically complex than their predecessors1, presenting unique challenges in both their stability and manufacturability. Accurate low volume subvisible particle measurements will form a critical aspect of the quality assessment of LNPs.&nbsp;Like all injectables, LNPs are subject to USP 787/788 SVP testing4 . However, USP 788 compendial Method 1, light obscuration (LO), is deemed “unsuitable to measure liposomal and colloidal suspensions” as stated in the chapter. In fact, USP 788 recommends membrane microscopy (Compendial Method 2) for measuring liposomal formulations, given LO’s inability to handle solutions with a complex matrix4. Aura uses Backgrounded Membrane Imaging (BMI), a form of membrane microscopy that enables high throughput, low volume subvisible particle characterization. In this application note, we demonstrate how Aura™ GT System can accurately and thoroughly characterize the subvisible particle content of LNPs with volumes as little as 25 µL per sample. We focus on the analysis of two LNP samples formulated in different buffers and subjected temperature and freeze thaw stresses. In addition, we use Aura GT’s SYBR™ Gold assay5 to help characterize nucleic acid escape in stressed LNP samples and quantitatively analyze the stability and purity of these samples.<h4>Experimental</h4><h5>Particle Measurements&nbsp;</h5>LNP samples were measured using BMI and Fluorescence Membrane Microscopy (FMM) using <a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/library?mainauthorItems=5&amp;search=aura+gt">Aura GT </a>on a black membrane plate. This procedure was adapted for each stress condition three wells were loaded with 25uL per well, and the filtrate stained with 1x SYBR Gold (2% v/v DMSO in PBS) for 1 min prior to FMM measurements. This procedure was adapted from Application note 16.5<h4>Conclusion&nbsp;</h4>Both samples A and B showed significant subvisible particle formation, more than 1x10^6/mL &gt;2 µm across most conditions except thermal stress, pointing to inherently unstable LNP formulations. Freeze thaw cycles significantly increased subvisible particle formation, while heat stress significantly reduced the subvisible particle concentration across both samples. Compared to protein formulations, this heat stress effect may appear unconventional. However, considering the LNP composition and upon further look at the literature, we are able to understand this phenomenon and conclude that significant heat stress can break a liposomal formulation apart3 , increasing the LNP solubility and thereby resulting in less insoluble particles captured on the membrane. On the other hand, freeze thawing produces more insoluble aggregates, thereby increasing subvisible counts as shown in BMI, exhibiting similar behavior to heat induced aggregation as in most protein formulations. A recurring theme in subvisible particle stability is that each formulation exhibits its own particle profile, LNPs are no exception. Another interesting data point is that freeze thawed LNPs showed significant SYBR Gold staining, whereas unstressed LNPs did not, indicating a unique nucleic acid leakage or rupture behavior for this type of stress. Finally, we also observed that buffer type did not significantly impact the subvisible particle count (data not shown). Whilst we observed significant particle counts across all samples tested, pH and buffer variance did not significantly increase particle formation. Indeed, several LNP formulations have reported robust stability profiles across a variety of buffers3 . Filtration of the final product may not be appropriate, as particle formation occurs following filtration, most likely in a concentration dependent manner (Figure 4). Multiple filtration steps, whilst able to clear the product, will undoubtedly result in reduced concentration of pharmacologically active LNPs and as a function of time particles will return as described in our “What Happens When I Filter My Sample” Application Note 21.&nbsp;In conclusion, Aura enables high throughput, low volume, accurate sub-visible particle analysis with direct applicability for LNP stability assessment. Arcane particle analysers, unsuitable for LNP assessment, will struggle to overcome the challenges associated with the physical and chemical complexity of LNPs. Indeed, Aura resolved these key challenges, providing a solution to sub-visible particle analysis of LNPs, from early stage inception through to product release.

News from LabRulezICPMS Library - Week 16, 2026

Article

Events

Application

Academy

Video

Food

RAFA provides an overview of contemporary trends in ANALYTICAL & BIOANALYTICAL STRATEGIES IN FOOD QUALITY AND SAFETY CONTROL and discusses CHALLENGES / NOVEL APPROACHES IN FOOD AND NATURAL PRODUCTS ANALYSIS.

Recent Advances in Food Analysis (RAFA)

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

Everything from the world of analytical chemistry in one place. We connect people in solving their problems. At Labrulez you will find all the necessary information easily, quickly and clearly. Stop searching and start finding.

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Thermo Scientific™ OXSAS™ X-Ray Fluorescence Analysis Software

Thermo Scientific™ OXSAS™ is a powerful and customizable XRF software that enables fast, template-driven analysis, automation, and standardless quantification options.

Enhance your lab efficiency and productivity with a customizable software solution that operates with XRF spectrometers. The flexible and powerful Thermo Scientific™ OXSAS™ X-ray Fluorescence Analytical Software performs rapid, high-quality sample analysis using template-driven operations.Optional standardless quantitative analysis packages offer additional versatility for labs analyzing a wide range of materials. This platform evolves to meet changing needs with up-to-date solutions throughout the instrument's lifetime.<h3>⚙️ Ease of Use</h3><ul><li>Integrated Analytical Assistant guides method creation/extension, suggesting optimal parameters for fast and accurate analysis.</li><li>Automatic Method Choice selects the best parameter set without user intervention.</li><li>Routine analysis requires minimal data-entry (e.g., just sample ID).</li><li>One-click batch creation for all samples requiring analysis.</li><li>Simple batch definition and management allows sample prioritization.</li></ul><h3>🖥️ Familiar User Interface</h3><ul><li>Comprehensive post-treatment of results, including export and Excel support.</li><li>Integrated Microsoft SQL Server Express database stores setups and data.</li><li>Export/import functions simplify transfer of standards, methods, or grades between instruments.</li><li>Regular software updates available from the OXSAS website.</li><li>Monitoring and maintenance tools help maximize system uptime.</li><li>Real-time integrated SPC (Statistical Process Control).</li><li>SCT Manager provides overview of instrument and method capability.</li><li>Measurement Uncertainty and Conformance Probability reporting for unknowns.</li></ul><h3>⚡Fast Calibration</h3><ul><li>Multiple analyte curve display, instant base curve calculation, calibration templates.</li><li>Multi-variable regression and correction models with integrated theoretical alpha calculation.</li></ul><h3>🧩 Available Options</h3>Optional standardless analysis packages for broader capability:<ul><li>Thermo Scientific™ QuantAS™ – Semi-quantitative analysis.</li><li>Thermo Scientific™ UniQuant™ – Analyze up to 79 elements in unknown samples without specific calibration, no certified reference materials needed.</li></ul><h3>🔧 Other Options</h3><ul><li>ARLcom: Result transmission via LAN/TCP/IP, serial, or to files.</li><li>Remote Sample Definition: Sample registration from external networked applications.</li><li>Automation: Supports Thermo Scientific SMS for fully automated analysis.</li><li>Charge correction: Calculates material weights needed to adjust out-of-spec charges.</li><li>SPC-Full: Full graphical package for online Statistical Process Control.</li></ul><h3>✅ Compatible with:</h3><ul><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/1211">Thermo Scientific™ ARL™ PERFORM'X Series</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products/1212">Thermo Scientific™ ARL™ OPTIM'X Series</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://icpms.labrulez.com/products?manufacturerItems=3&amp;search=9900">Thermo Scientific™ ARL™ 9900 IntelliPower Series</a></li></ul>

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News from LabRulezICPMS Library - Week 16, 2026

RAFA 2026 - Registration & Call for Abstracts are now OPEN

Proficiency testing schemes and other interlaboratory comparisons