<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

44th International Symposium on Capillary Chromatography - Invited speakers

Article

Events

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

ISCC & GC×GC Symposium bring together global experts to discuss advances in capillary and multidimensional chromatography, mass spectrometry, and analytical technologies for complex sample analysis.

International Symposium on Capillary Chromatography (ISCC) and GCxGC Symposium

Agilent Technologies

Phenomenex

Thermo Fisher Scientific

SelectScience

Waters Corporation

<div>Downstream process development usually requires numerous iterations until optimization is achieved. Offline analytics are often a bottleneck for timely development. The antidote to lagging offline analytics is inline or online process analytical technology (PAT).Real-time multi-angle light scattering (RT-MALS) is a PAT that monitors fundamental biophysical product attributes like molar mass, size and titer, every second during downstream operations such as FPLC or UF/DF. For AAVs, RT-MALS also monitors the full capsid ratio. This webinar describes the technology of RT-MALS and its implementation with a variety of bioprocess unit operations and modalities, from proteins to viral vectors, LNPs and pneumococcal vaccines.<h4>In this webinar, you will learn:</h4><ul><li>What are the CQAs and other attributes determined by RT-MALS for different modalities</li><li>How RT-MALS accelerates bioprocess DSP development</li><li>How process control with RT-MALS can enhance yield and lot consistency</li></ul><h4>Who Should Attend:</h4><ul><li>PAT experts for biologics, vaccines and gene therapies</li><li>Biopharm process development scientists</li><li>Downstream bioprocess engineers</li><li>Biopharm MSAT leaders</li></ul><blockquote>Presenter: Dan Some, Ph.D. (Sr. Principal Scientist, Waters | Wyatt Technology)Dr. Daniel Some is a Sr. Principal Scientist at Waters | Wyatt Technology, where he contributes to product and application development as well as scientific and technical marketing. Currently he leads Wyatt’s program for commercializing real-time MALS PAT products.</blockquote></div>

Waters Corporation: Accelerating Downstream Process Development for Biologics, Gene Vectors and Vaccines

Accelerating Downstream Process Development for Biologics, Gene Vectors and Vaccines

This webinar describes the technology of RT-MALS and its implementation - proteins, viral vectors, LNPs and pneumococcal vaccines.

Accelerating Downstream Process Development for Biologics

Gel Permeation Chromatography/Size Exclusion Chromatography (GPC/SEC) is a non-interactive chromatographic technique that separates polymer samples based on their size in solution, rather than their chemistry. &nbsp; Developing a GPC/SEC method involves several key steps to ensure accurate and reproducible results.In this e-Seminar, we will explore the key parameters of GPC/SEC method development:<ul><li>Identify the Polymer Sample: Understanding the type of sample.</li><li>Solvent Choice: Deciding between organic and aqueous solvents.</li><li>Column Selection:&nbsp; Considerations for packing type, particle size, and pore size. &nbsp;Learn how to maximize column performance through selection.</li><li>Calibration: Choosing appropriate standards and understanding their significance.</li><li>Optimize the System: &nbsp;Considerations for flow rate, temperature, and injection volume</li><li>Detection: Utilizing refractive index (RI) and advanced detection methods.</li></ul>We will delve into each of these areas in detail, offering technical insights, application examples, and share valuable tips to help you develop a GPC/SEC method that is both robust and reproducible. &nbsp;<blockquote>Presenter: Jean Lane (Application Engineer, Agilent Technologies, Inc.)Jean has been employed with Agilent since Nov 2010 in technical and applications support and has a primary role supporting Agilent’s full line of LC columns and consumables, which also includes support for Agilent’s GPC/SEC product line. She came to Agilent thru acquisition of Varian and the former Polymer Laboratories. Jean has 20 plus years of technical and applications support for both HPLC and GPC consumable products. In addition to practical chromatography experience in the laboratory, she has had many, many years in her technical role involving customer support providing assistance and troubleshooting for customer chromatography issues.</blockquote>

Agilent Technologies: A Systematic Approach to GPC/SEC Method Development

A Systematic Approach to GPC/SEC Method Development

In this e-Seminar, we will explore the key parameters of GPC/SEC method development:

In Part 1 of this workshop, we discuss the capabilities of the Praying Mantis accessory from Specac/Harrick in combination with the Cary 5000 UV-VIS/NIR System. &nbsp;It is a critical accessory for assessing the diffuse reflectance of small volumes of powders. &nbsp;Additional sampling capabilities through specialized reaction chambers allow for the control of sample pressure, temperature, and environment for catalyst studies.<blockquote>Presenter: Scott Melis, PhD (Application Scientist, Agilent Technologies, Inc.)Scott Melis has a PHD in Physics from Georgetown University in Washington, DC and started with Agilent in 2021 as a Molecular Spectroscopy Application Scientist. In his graduate work, Scott studied nanoparticle formation and growth for a variety of applications. Projects that he worked with include developing processes to deposit and characterize semiconducting molecular nano-cocrystals for use in optoelectronic devices as well as controlling polymer nanoparticle size through rapid mixing conditions.</blockquote>

Agilent Technologies: Optimize your FTIR, UV-Vis-NIR, Raman, Imaging, and Fluorescence Workflows

Part 1: Characterizing catalysts using an UV-VIS/NIR system with the Praying Mantis diffuse reflectance accessory.

Part 1 discusses the capabilities of the Praying Mantis accessory (Specac/Harrick) in combination with Cary 5000 UV-VIS/NIR System.

Catalyst Analysis with UV-VIS/NIR & Praying Mantis DR

The efficiency and reliability of lithium-ion batteries are significantly impacted by the detailed composition and impurities of their electrolytes. This webinar focuses on the comprehensive characterization of both major components and impurities in these electrolytes through the use of gas chromatography mass spectrometry (GC-MS), ion chromatography mass spectrometry (IC-MS), and inductively coupled plasma mass spectrometry (ICP-MS). GC-MS enables the separation and detection of volatile organic compounds, IC-MS detects ionic compounds, and ICP-MS detects trace metal impurities.The combined data from these techniques offer a thorough understanding of the electrolyte, which is crucial for enhancing battery performance and lifespan. Drawing upon our extensive experience in battery technology, we will present case studies and experimental findings that demonstrate the necessity of this integrated analytical approach.There will also be the opportunity for a live Q&amp;A with the speakers.&nbsp;Learning points:<ul><li>Characterisation of electrolytes in lithium-ion batteries&nbsp;</li><li>Role of analytical instrumentation in characterization of electrolytes.&nbsp;</li><li>Understanding of IC-MS, GC-MS and ICP-MS in electrolyte characterisation&nbsp;</li></ul>Who should attend:<ul><li>Researchers in the field of lithium-ion batteries&nbsp;</li><li>Manufacturers of lithium-ion batteries&nbsp;</li><li>Users of analytical instruments in the battery market&nbsp;</li></ul><blockquote>Presenter: Dr. Daniel Kutscher (Manager Product Applications, TEA, Thermo Fisher Scientific)Dr. Daniel Kutscher manages the Application Development for trace elemental analysis and GC/GC-MS products at Thermo Fisher Scientific. After graduation in Chemistry in 2007, Daniel obtained his PhD from the University of Oviedo in 2011. In the same year, he joined Thermo Fisher Scientific and has had different roles in application development and marketing.Presenter: Dr. Simon Göckler (Market Sales Specialist – Clean Energy, Thermo Fisher Scientific)Dr. Simon Göckler, Market Sales Specialist for Clean Energy/EMEA at Thermo Fisher Scientific, graduated with a degree in food chemistry in 2005 and earned his PhD in 2009 at KIT. He joined Dionex the same year, gaining extensive experience in ion chromatography and other chromatography techniques. Simon has held various roles in instrument sales and business development. At Thermo Fisher, he focuses on the clean energy market, leveraging his expertise to drive growth and innovation.Presenter: Dr. Timothy Cross (Senior Manager, EMEA Regional Marketing, Thermo Fisher Scientific)Dr. Timothy Cross, Senior Manager of EMEA Regional Marketing at Thermo Fisher Scientific, graduated with a degree in Biology in 1995 and an MSc in Immunology in 1996 before subsequently earning his PhD in Immunology at the University of Birmingham, UK Following a short spell in proteomics R&amp;D, he has undertook a number of marketing roles in life and analytical science markets, joining Thermo Fisher Scientific in 2014, initially as Regional Marketing Manager for HPLC and CDS Software.</blockquote>

Thermo Fisher Scientific: Comprehensive characterization of electrolytes in lithium-ion batteries

Comprehensive characterization of electrolytes in lithium-ion batteries

This webinar focuses on characterization of components and impurities in Li-ion-batteries electrolytes by GC-MS, IC-MS, and ICP-MS.

Characterization of electrolytes in lithium-ion batteries

<h4>Overview</h4>This webinar, co-hosted by Phenomenex and the Bio-Analytical Separation Science Group at Vrije Universiteit Brussel, will cover:<ul><li>The growing potential of oligonucleotide therapeutics and the importance of thorough impurity profiling.</li><li>Challenges in detecting critical impurities such as shortmers and phosphodiesters (PO) during synthesis.</li><li>Ion-pair reversed-phase liquid chromatography’s (IP-RPLC) mechanism of action for high-resolution impurity analysis.</li><li>Evaluating the impact of column preheaters on analyte dispersion and method performance.</li><li>The role of fluoroalcohols in enhancing LC separation and MS detection.</li><li>Comparing bio-inert columns for improved impurity profiling outcomes.</li></ul><h4>Key Learning Points</h4><ul><li>Understand the therapeutic mechanisms of oligonucleotides and the significance of base, ribose, and phosphate modifications.</li><li>Recognize the analytical challenges in oligonucleotide impurity profiling, including shortmers and phosphodiester impurities.</li><li>Learn how to develop and optimize IP-RPLC-MS methods for high-throughput analysis.</li><li>Evaluate the influence of preheater effects and fluoroalcohols on separation and detection sensitivity.</li><li>Compare the performance of bio-inert columns for impurity profiling.</li></ul><h4>Who Should Attend</h4><ul><li>Oligonucleotide Researchers: Ideal for scientists involved in developing and characterizing oligonucleotide therapeutics.</li><li>Analytical Chemists: Professionals focused on impurity profiling and method optimization using advanced chromatographic techniques.</li><li>Biopharmaceutical Quality Control Experts: Valuable for those ensuring the purity, stability, and safety of oligonucleotide-based therapeutics.</li><li>Contract Research Organizations</li><li>Biopharmaceutical Innovator Companies</li></ul><blockquote>Speaker: Dr. Sebastiaan Eeltink &nbsp;(Professor and lead investigator of the Eeltink Laboratory at the University of Brussel &amp; Editor of Analytical Science Advances at Wiley)Dr. Sebastiaan Eeltink is a Full Professor and lead investigator of the Eeltink Laboratory at the University of Brussel and an Editor of Analytical Science Advances at Wiley. His team focuses on developing and designing novel analytics for the high-resolution profiling of biomolecules and biomolecular interactions using ultrahigh-pressure liquid chromatography (UHPLC) and multi-dimensional liquid chromatographic workflows with mass spectrometry (MS) detection. In addition, his team also manages the University’s proteomics platform which offers high-performance LC-MS proteomics profiling expertise and advise to academic and industrial collaborators.Speaker: Quang-Dong Bui &nbsp;(PhD student at University of Brussels)Quang-Dong Bui is currently a PhD student at University of Brussels under the supervision of Professor Sebastiaan Eeltink, where he develops analytical methods for key oligonucleotide projects and is an active scientist in the oligonucleotide and mRNA research community.</blockquote>

Phenomenex: Advanced IP-RPLC-MS Strategies for High-Resolution Oligonucleotide Impurity Profiling

Advanced IP-RPLC-MS Strategies for High-Resolution Oligonucleotide Impurity Profiling

Discover advanced IP-RPLC-MS methods for high-resolution oligonucleotide impurity analysis. Enhance your analytical workflows and data precision.​

Advanced IP-RPLC-MS for Oligonucleotide Profiling

<div><div container-id="cq-colctrl-lt0" comp-id="A1"><div><h4>Lessons learned in developing an ion pair free, compliant workflow for ASO RNA impurity analysis</h4>Join this live webinar with Dr. Ken Cook and discover innovative techniques for oligonucleotide impurity quantitation, automation, and data handling to enhance your laboratory's efficiency and compliance.<h5>Topics:</h5><ul><li>Ion pair free separation mechanisms<ul><li>Reasons for choosing the best path for quantitative methods.</li></ul></li><li>Removing problems of adducts and in-source induced impurities<ul><li>Preventing accurate quantitation of real impurities.</li></ul></li><li>Choice of the best charge states to use for quantitation</li><li>Deconvolution and XIC Component Tables in Thermo Scientific Chromeleon Software<ul><li>Compliant data handling and complementary techniques.</li></ul></li><li>Automation of Annotation, Integration, and Compliant Reporting<ul><li>UV and MS data handling to remove bottlenecks in developing and running new quantitative methods for oligonucleotide impurity analysis</li></ul></li></ul>After the presentation, we planned time to answer your questions.<h5>Who should attend?</h5><ul><li>Laboratory managers or analysts<ul><li>developing methods for new synthetic therapeutic oligonucleotides</li><li>implementing methods for existing modalities</li></ul></li><li>Laboratories<ul><li>involved in clinical trial analysis</li><li>aiming to avoid ion pair contamination in their LC-MS systems</li></ul></li><li>Oligonucleotide analysts in R&amp;D or QC departments</li><li>Analysts looking for green oligonucleotide chemistry</li></ul>You cannot attend the live broadcast on May 22? Please register to automatically receive an email with the link to the recording.<blockquote>Presenter: Dr. Ken Cook (Applications Scientists Manager, Thermo Fisher Scientific)Moved to industry from a University lectureship in Biochemistry, University of Newcastle upon Tyne, following 7 years’ experience in academia. Now with over 35 years’ experience with Thermo Fisher Scientific using a wide range of analytical equipment and software. Publications range from metabolomics, proteomics to large biopharmaceutical drug analysis. Current job title is the European manager for the BioPharma expert support group. This involves the support of Bio-Pharmaceutical applications to characterise protein and oligonucleotide based bio-therapeutics. This involves ongoing collaborations with the Biopharmaceutical industry and academia. Characterization methods of Bio-therapeutics include, monoclonal antibodies, peptides, AAV analytical development, small and large RNA analysis including sequence mapping of mRNA by LC/HRMS.</blockquote></div></div></div>

Thermo Fisher Scientific: ASO RNA impurity analysis

ASO RNA impurity analysis

Discover innovative techniques for oligonucleotide impurity quantitation, automation, and data handling to enhance your laboratory's efficiency and compliance.

<div><div container-id="cq-colctrl-lt0" comp-id="A1"><div>When looking for new ways to increase sample throughput in proteomics, without compromising on proteome profiling or quantitation, Thermo Scientific Vanquish Neo UHPLC systems and Thermo Scientific µPAC Neo columns can really make a difference.Using the Vanquish Neo system, with its newly introduced tandem workflow, a dual separation workflow in a single system is created to maximize MS utilization for high-throughput and deep-dive proteomics.Benefiting from the perfectly ordered microfabrication of the Thermo Scientific™ µPAC™ Neo columns, this workflow has advanced proteomics research into the next era with maximal reproducibility and robustness.Join this free webinar to learn more about how you can employ Vanquish Neo Tandem Workflow systems and µPAC Neo columns in your lab.In this webinar, we present to you how to meet increasing sample queue demands without compromising separation and MS results by:<ul><li>using the Vanquish Neo UHPLC system for low-flow separations in proteomics</li><li>maximizing mass spectrometer utilization with the Vanquish Neo Tandem Direct-Injection workflow for increased sample throughput, and minimized column carryover</li><li>Tandem Direct-Injection workflow for nano, capillary and micro-flow applications</li><li>utilizing the unique micro-pillar array backbone to provide both, highest robustness and consistency</li></ul>Cannot join on May 20? Please register anyway to automatically receive the link to the recording.<blockquote>Presenter: Robert van Ling (Product Manager Low-flow HPLC Columns, Thermo Fisher Scientific)Experienced marketeer &amp; business developer, as well as technical sales support specialist, for the biopharma and omics community. 25+ years of protein, peptide and RNA chromatography and LC/MS experience, focused on providing researchers with innovative and high-performance workflows and solutions.</blockquote></div></div></div>

Thermo Fisher Scientific: Innovative separation approaches for MS-based proteomics

Innovative separation approaches for MS-based proteomics

Join this free webinar to learn more about how you can employ Vanquish Neo Tandem Workflow systems and µPAC Neo columns in your lab.

<div><div container-id="cq-colctrl-lt0" comp-id="A1"><div>Halogens like fluorine, chlorine, bromine, and iodine, along with sulfur, are corrosive and hazardous elements that pose significant environmental and industrial challenges. Accurate monitoring of these elements is crucial to protecting human health and ensuring efficient manufacturing processes. Traditional methods often struggle to detect these analytes in complex samples such as petrochemicals and personal care products, complicating quality control and assurance efforts.Join us for an exclusive product launch webinar where three experts from Thermo Fisher Scientific will introduce an innovative Combustion-Ion Chromatography (C-IC) system. This cutting-edge technology is designed to enhance your halogen analysis, streamline your workflow, improve data accuracy, and deliver exceptional precision and efficiency.Gain valuable insights from Dr. Carl Fisher, Pavan Sandhu, and Dr. Neil Rumachik as they discuss the advanced features, operational benefits, and application performance of this new C-IC system.<h5>Key learning objectives</h5><ul><li>Gain a comprehensive understanding of the features and benefits of the new C-IC system</li><li>Explore the enhanced capabilities and diverse applications of the system across various industries</li><li>Discover how this system can optimize your workflow and significantly improve data accuracy</li></ul><h5>Who should attend?</h5><ul><li>Laboratory managers, directors, quality control and assurance professionals</li><li>Environmental scientists, analytical chemists, technicians and researchers</li><li>Professionals in the consumer product manufacturing, power generation, food, and chemical industries</li></ul><h4>In a different time zone?</h4>This webinar is one of three sessions that are taking place over different time zones. This webinar has been specifically scheduled for the European time zone. Please use the links provided to access the session that best suits your region:<ul><li><a target="_blank" rel="noopener noreferrer" href="https://www.selectscience.net/webinar/spark-new-insights-boost-your-lab-s-power-with-combustion-ion-chromatography">USA</a></li><li><a target="_blank" rel="noopener noreferrer" href="https://www.selectscience.net/webinar/spark-new-insights-boost-your-lab-s-power-with-combustion-ion-chromatography-asia">Asia</a></li></ul><h5>Certificate of attendance</h5><ul><li>All webinar participants can request a certificate of attendance, including a learning outcomes summary, for continuing education purposes.</li><li>If you view the on-demand webinar, you can request a certificate of attendance by emailing editor@selectscience.net.</li></ul><blockquote>Presenter: Dr. Carl Fisher (Product Marketing Manager, Thermo Fisher Scientific)Dr. Carl Fisher is a Product Marketing Manager at Thermo Fisher Scientific. He earned his PhD in Biochemistry from the University of Alberta in Edmonton, AB, which was followed by a post-doctoral fellowship at Brigham and Women’s Hospital, Harvard Medical School in Boston, MA. After joining Thermo Fisher Scientific, he spent several years in the Applications Development team as an analytical chemist, producing technical and application notes. In his current role, he drives the delivery of Ion Chromatography and sample preparation solutions for the environmental and industrial markets.Presenter:&nbsp;Pavan Sandhu (Product Management Specialist, Thermo Fisher Scientific)Pavan Sandhu completed her MS in Biomedical Engineering from University of Texas at Dallas and has several years of experience in clinical diagnostics and analytical instrumentation. At present, she is the Product Management Specialist in the Ion Chromatography &amp; Sample preparation (IC/SP) business unit at Thermo Fisher Scientific, managing Combustion IC &amp; Discrete Analyzer products. Prior to joining IC/SP, she was part of an R&amp;D team at Thermo Fisher’s Clinical Diagnostic Division (CDD) leading product development and design transfer of multiple diagnostic products.Presenter:&nbsp;Dr. Neil Rumachik (Applications Development Manager, Thermo Fisher Scientific)Dr. Neil Rumachik completed his graduate studies in Chemistry at the University of California, Berkeley (MS), and Stanford University (PhD) under the mentorship of Professor Carolyn Bertozzi before joining Thermo Fisher Scientific. He currently works as the Manager of Applications Development in the Ion Chromatography and Sample Preparation business unit at Thermo Fisher Scientific. Before moving to the apps team, he worked as a staff scientist in R&amp;D at Thermo Fisher, where he developed IC-MS products and workflows for carbohydrate analysis. With over a decade of experience at the intersection of chemistry and biology, he is focused on developing cross-disciplinary methods and utilizing multi-omics platforms to advance biological studies.Moderator: Cameron Smith-Craig (Pharma and Applied Sciences Editor, SelectScience)</blockquote></div></div></div>

Thermo Fisher Scientific: Spark new insights - Boost your lab's power with combustion-ion chromatography

Spark new insights - Boost your lab's power with combustion-ion chromatography (Europe)

Experts from Thermo Fisher Scientific will introduce an innovative Combustion-Ion Chromatography (C-IC) system. 

Boost your lab's power with combustion-ion chromatography

<div><div container-id="cq-colctrl-lt0" comp-id="A1"><div>Join us for an exclusive opportunity to connect directly with Thermo ScientificTM ChromeleonTM Chromatography Data System (CDS) product experts in this interactive webinar session focused specifically on data processing and data reporting. This interactive session brings together specialists from our product marketing and product management teams to address your Chromeleon challenges and help you maximize the platform's capabilities.The heart of this webinar is live software demonstrations, where our experts will show you exactly how to implement solutions within Chromeleon CDS. Watch as they navigate the software in real-time, revealing practical techniques to enhance your laboratory workflows.This session will be driven by you — our users! &nbsp;Bring your questions about:<ul><li>Data processing strategies and best practices</li><li>Custom report creation and template design</li><li>Statistical analysis tools and calculations</li><li>Data visualization techniques</li></ul>Submit your questions early! Questions submitted prior to 7 May will be prioritized, giving you the best chance to have your specific challenges addressed during the webinar.Whether you're looking to solve specific challenges or simply enhance your Chromeleon expertise, this interactive Q&amp;A session will provide valuable insights directly applicable to your daily work.<blockquote>Presenter: Barbara van Cann (Senior Manager, Product Management, Thermo Fisher Scientific)Barbara van Cann holds a Bachelor of Science in Analytical Chemistry and has accumulated over 25 years of experience at Thermo Fisher Scientific (Dionex). Her extensive background encompasses analytical chemistry, chromatography hardware, and computer software.Throughout her career, Barbara has held various roles within the Dutch sales organization, including IC Application Chemist and Sales Support for HPLC and Chromeleon software. She later transitioned to the Chromeleon team, where she currently serves as the Senior Manager for Product Management within the CMD Software organization. In this capacity, Barbara is responsible for identifying customer requirements for Chromeleon CDS, driving roadmap planning, and developing product strategies to maximize customer value and impact.Presenter:&nbsp;Peter Sauter (Product Manager, Thermo Fisher Scientific)Graduated in 1986 with a Diploma in Mathematics at the University in Ulm / Germany.Joined Softron in 1986 which later became Gynkotek/Softron and Dionex/Softron (now as part of Thermo Fisher Scientific) and worked over the past almost 40 years as a developer, R&amp;D manager and nowadays as product manager in the development of various chromatography data systems and customer specific Addons such as Kontron Datasystem 420, &nbsp;GynkoSoft, Chromeleon 6 and Chromeleon 7. &nbsp;Presenter:&nbsp;Anthony Crawshaw (Product Manager, Thermo Fisher Scientific)Graduated in 1997 with an BSc in Applied Chemistry from Sheffield Hallam University. &nbsp;Subsequently worked in Pharmaceutical Contract Research Organisations (Aptuit and Almac). &nbsp;This varied from Pharmaceutical Analysis labs, through to method development and validation. &nbsp; Joined Dionex (later to become Thermo Fisher Scientific) in 2011 as a Sales Support Specialist, supporting the UK sales teams with both HPLC Hardware and applications, as well as Chromeleon and Chromeleon Enterprise support. &nbsp;This involved the management and deployment of the Chromeleon Enterprise systems within the UK at customer sites. &nbsp;In 2018, transitioned to the newly formed Global eCDS team, supporting EMEA. &nbsp;This solely focused on Chromeleon and Chromeleon Enterprise deployments. &nbsp;In 2022, transitioned into Product Management as the PM for Chromeleon Enterprise.Presenter:&nbsp;Darren Barrington-Light (Senior Manager, Product Marketing, Thermo Fisher Scientific)Darren has worked for over 30 years with Chromatography Data Systems and for over 25 years with Chromeleon CDS. He has a unique understanding of the requirements of organizations that rely on data to manage their day to day operations. &nbsp;As capabilities have advanced, Darren has worked with clients across multiple industries to show them how enterprise-level software can help them to improve their day to day operations and drive fast, informed decisions.Presenter:&nbsp;Zoe Julian (Product Marketing Manager, Chromatography Software, Thermo Fisher Scientific)With over 12 years of experience working with chromatography and mass spectrometry techniques with a background in GC and GC-MS(/MS) organic environmental analysis, Zoe Julian has helped many laboratories and industries improve workflows through a unique understanding of their challenges. Transitioning to a focus on Thermo Scientific Chromeleon CDS, she has shown customers how software solutions can improve their productivity and support their day-to-day operations.Presenter:&nbsp;Laércio Fernandes (Product Marketing Manager, Chromatography Software, Thermo Fisher Scientific)With a background rooted in analytical chemistry, sales, and support, Laércio Fernandes has over 15 years of experience in the analytical field and has worked in constant connection with Thermo Scientific Chromeleon CDS and chromatography instrumentation with a focus on ion chromatography, IT, and Cloud. His background in sales and support has enabled his good overview and understanding of different processes and challenges that laboratories may face. This has allowed him to better support customers to improve their workflows and productivity.&nbsp;</blockquote></div></div></div>

Thermo Fisher Scientific: Let’s Talk Chromeleon: Interactive Q&A with Product Experts

Let’s Talk Chromeleon: Interactive Q&A with Product Experts

Exclusive opportunity to connect directly with Thermo Scientific Chromeleon Chromatography Data System product experts in interactive webinar session.

In this webinar we will explore the Merel, dissoBOT system, a pioneering technology in the pharmaceutical testing landscape, introducing the first fully automated dissolution system featuring clip-on/off capabilities.This state-of-the-art system simplifies the dissolution process by enabling automatic sequential operations—cleaning, media dispensing, and sample introduction without interfering with the ongoing dissolution process. Designed to work seamlessly with established systems such as the Agilent 850-DS Dissolution Sampling Station and the 708-DS Dissolution Apparatus, dissoBOT enhances efficiency and reproducibility. The advanced automation facilitated by collaborative robotics allows for extended operational cycles and minimal setup time, with a clip-on procedure completing in less than a minute.This webinar will detail the operational principles, components like the Dosage Delivery Module (DDM), and the integration capabilities of the dissoBOT with current dissolution apparatuses, ensuring precise media dispensing and accurate sample analysis. Participants of this webinar will gain in-depth knowledge and practical insights into the automation of the dissolution testing process using the Merel dissoBOT system.<h5>Key learning objectives include:</h5><ul><li>Understanding the foundational technology behind the dissoBOT's clip-on/off capability and its integration with existing dissolution systems.</li><li>Exploring the automated functions of the dissoBOT, including sequential media dispensing, cleaning, and sample introduction, and how these operations enhance testing efficiency and accuracy.</li><li>Learning about the compatibility of the dissoBOT with common dissolution apparatuses like the Agilent 708-DS and the 850-DS Dissolution Sampling Station.</li><li>Gaining insights into the process enhancements brought by the dissoBOT, such as reduced manual intervention, increased reproducibility, and streamlined workflow.</li><li>Discovering the technical specifics of the system components, including the Dosage Delivery Module, dissoDOSE technology, and automated sample collection methods.</li><li>Understanding the impact of dissoBOT on pharmaceutical quality control and how it can lead to more reliable and faster dissolution testing results.</li></ul><blockquote>Presenter: Owain McKenzie (Dissolution Business Team Manager EMEA, Agilent Technologies)Owain McKenzie is currently the EMEA Dissolution Business Team Manager with Agilent. Since 2000 Owain has performed analytical testing, supervised pharmaceutical laboratories, run sales teams, and managed customer support teams with GSK, VanKel, Erweka, Varian and Agilent. Primary responsibilities have been in the fields of product release, stability, product development and support, LC, MS &amp; UV. Dissolution method development and validation, instrument qualification and calibration, technology transfers and training. Current activities since 2010 have focused on providing method and technical application support for dissolution and drug release testing in the pharmaceutical industry as well as Agilent R&amp;D, Marketing and Sales teams. Owain provides numerous talks and publications on dissolution related techniques and topics including publication of the Immediate Release Newsletter, and Dissolution Discussion Group (DDG). He received his MSc degree in Chemistry from the University of Leeds, UK, and is an active member of both the Royal Pharmaceutical Society and the Royal Society of Chemistry in London UK.Presenter: Nejc Zorko Horvat (Product Manager, Merel)Nejc Zorko Horvat has been working in the field of dissolution, UV-Vis-NIR, and fluorescence spectroscopy for 15 years. He manages domestic and international projects, including installation, qualification, and customer training on novel and complex systems. With extensive experience supporting customers in GMP environments and numerous compliance trainings, his main focus is on the pharmaceutical market.His background in IT allows him to provide solutions for both hardware and local or networked software. Since 2024, he has been managing the complete portfolio of Merel Instruments in foreign markets. His role includes presenting at international seminars, fairs, and specialized events, conducting online product demos, managing dealers, and visiting customers.</blockquote>

Agilent Technologies: Automation Of Dissolution Process With The Merel dissoBOT System

Automation Of Dissolution Process With The Merel dissoBOT System

In this webinar we will explore the Merel, dissoBOT system, a pioneering technology in the pharmaceutical testing landscape

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