In the week of February 23, the following webinars await you in the field of gas / solid phase and especially Raman, FTIR, GC and GC/MS.<blockquote><h4><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinars">👉 DETAILS AND REGISTRATION IN THE WEBINARS SECTION</a></h4>👉 Search and filter in the largest global database with over 5 500 GC, LC, MS and spectroscopy webinars.</blockquote><div><div><div><div><div><div><h5>1. Technology Networks: Real-Time In-Line Insight for Therapeutic Protein Production</h5><ul><li>Tu, 24.2.2026 16:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5796">Registration</a></li></ul>Discover how real-time, in-line Raman monitoring improves control and consistency in therapeutic protein manufacturing by delivering actionable insights across downstream operations.<h5>2. Agilent Technologies: Microplastics in Wastewater – A Population Based Approach to Identifying Potential Sources</h5><ul><li>Tu, 24.2.2026 21:30 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/2531">Registration</a></li></ul>Using LDIR within a closed wastewater treatment system, this webinar explores how microplastics are quantified at multiple treatment stages to identify potential contamination sources.<h5>3. Separation Science: PFAS in Air – A Practical Toolkit for Real-World Applications</h5><ul><li>Th, 26.2.2026 11:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5812">Registration</a></li></ul>Discover practical solutions and emerging approaches for monitoring volatile and semi-volatile PFAS in air and materials.<h5>4. Waters Corporation: GC-MS/MS Under Atmospheric Pressure – Benefits for Dioxin and Pyrethroid Analysis</h5><ul><li>Th, 26.2.2026 15:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5919">Registration</a></li></ul>Learn how environmental labs can adapt to revised EU Water Framework Directive requirements, address pollutants like PFAS and dioxins, and leverage GC-MS/MS innovations.<h5>5. LECO: Advanced GC×GC-MS Strategy for Pesticide Analysis in a Highly Complex Chili Pepper Matrix</h5><ul><li>Th, 26.2.2026 16:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5760">Registration</a></li></ul>Discover how GC×GC-MS enables reliable determination of pesticide residues in complex chili pepper matrices by overcoming severe interferences that limit conventional GC-MS/MS.<h5>6. SelectScience: The PFAS Measurement Crisis – A Roundtable Discussion</h5><ul><li>Fr, 27.2.2026 17:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5841">Registration</a></li></ul>Join this expert roundtable to discuss limitations of targeted PFAS methods, non-targeted analysis strategies, next-generation standards, and closing the PFAS data gap.</div></div></div></div></div></div>

Webinars LabRulezGCMS Week 09/2026

This study evaluates the in vitro antibacterial potential of Pinus nigra and Thymus serpyllum essential oils, individually and in combination, against 12 human pathogens. Antimicrobial activity and synergistic interactions were assessed using microdilution and checkerboard assays, with additional testing alongside ciprofloxacin, amoxicillin, and tetracycline.The oil combination showed strong synergy against Enterococcus faecalis and Staphylococcus epidermidis, while P. nigra combined with amoxicillin was synergistic against Streptococcus mitis. Major oil components were characterized by GC/MS and GC/FID, and cytotoxicity testing confirmed no toxicity for synergistic combinations. These findings highlight the potential of essential oil–antibiotic combinations in antibacterial strategies.<blockquote><h4>The original article</h4><h4><a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c07183">In Vitro Antibacterial Potential of Pinus nigra-Thymus serpyllum Essential Oil and Antibiotic Combinations</a></h4>Sümeyye Elif Kahya*, Ayşe Esra Karadağ, Betül Demirci, and Fatih Demirci*ACS Omega 2025, 10, 50, 61528–61534<a target="_blank" rel="noopener noreferrer" href="https://doi.org/10.1021/acsomega.5c07183">https://doi.org/10.1021/acsomega.5c07183</a><h6>licensed under <a target="_blank" rel="noopener noreferrer" href="https://creativecommons.org/licenses/by/4.0/">CC-BY 4.0</a></h6></blockquote>Selected sections from the article follow. Formats and hyperlinks were adapted from the original.<div>Thymus serpyllum L. (Lamiaceae) is commonly known as a ‘wild thyme’, and is originally from Eastern Mediterranean regions, where also a monograph of the dried flowering aerial parts in the European Pharmacopoeia exists as Serpylli herba, which is widely used in Europe. <a href="javascript:void(0);">(1)</a> Carvacrol was reported as the main component in T. serpyllum, with variable amounts of thymol, linalool, linalyl acetate, borneol, 1,8-cineole, germacrene D, p-cymene, γ-terpinene, myrcene, and β-caryophyllene, respectively. The content varies significantly based on the species, genetic variation, developmental stage, origin, and cultivation conditions, so its chemotype diversity occurs. <a href="javascript:void(0);">(2,3)</a> Its preparations are traditionally used for treating colds, rheumatism, sciatica, and its stimulating, disinfectant, and immune-stimulating effects. <a href="javascript:void(0);">(4,5)</a>Pinus nigra JF Arnold (Black pine) is a diverse species which belongs to the Pinaceae family, present throughout the Mediterranean region. <a href="javascript:void(0);">(6)</a> The species is divided into seven subspecies: Pinus nigra subsp. dalmatica (Vis.) Franco, P. nigra subsp. laricio Palib. ex Maire, P. nigra subsp. nigra, P. nigra subsp. pallasiana (Lamb.) Holmboe, P. nigra subsp. salzmannii (Dunal) Franco, P. nigra f. seneriana (Saatçioglu) Kandemir &amp; Mataraci, and P. nigra var. yaltirikiana Alptekin. <a href="javascript:void(0);">(7)</a> Black pine is recognized for its genetic, morphological, phenotypic, and biochemical diversity. The chemical composition of essential oils varies among different origins and subspecies, with the abundance of monoterpenes such as α-pinene, β-pinene, limonene, δ-3-carene, and β-phellandrene among others. <a href="javascript:void(0);">(8,9)</a> Biological activities such as antibacterial, antifungal, and antioxidant are reported within traditional medicine. <a href="javascript:void(0);">(10)</a>Antimicrobial resistance can be classified as one of the clinical and economical devastating impacts globally. Pathogens such as Staphylococcus aureus and Pseudomonas aeruginosa are frequently listed as priority pathogens by the World Health Organization, because they rank as leading causes for infections acquired in communities along with hospitals worldwide. <a href="javascript:void(0);">(11,12)</a> According to the One Health approach, the spread of resistant strains constitutes a significant threat to human, animal, and environmental health. Consequently, new research for new innovative antimicrobial agents such as essential oils and combinations withdraw attention as a sustainable strategy. <a href="javascript:void(0);">(13)</a>The combination of conventional antibiotics with EOs enhances their effectiveness, positioning EOs as promising alternatives to synthetic antimicrobial agents for combating resilient infections, where recent studies demonstrated synergistic activity in specific combinations. <a href="javascript:void(0);">(14,15)</a> Synergistic effects have significant advantages, such as the drug combination exerting a more substantial impact than the sum of the drugs’ effect, lower toxicity, and reduced side effects. <a href="javascript:void(0);">(16)</a>In this present study, to achieve synergistic antimicrobial activity T. serpyllum and P. nigra essential oil combinations were systematically evaluated. The checkerboard method was used to evaluate the binary combinations of the essential oils and their individual combinations with tetracycline, amoxicillin, and ciprofloxacin, respectively. In addition, based on the GC/MS and GC/FID verification results, the combinations of the major components geraniol and α-pinene were evaluated against pathogenic microorganisms. To the best our knowledge, the combination of T. serpyllum and P. nigra essential oils, tetracycline, amoxicillin, ciprofloxacin, major components geraniol and α-pinene, respectively, were evaluated for the first time. Also, the active combinations were further assessed for their potential toxicity using the in vitro MTT assay.<h4>2. Result and Discussion</h4><h5>2.1. Phytochemical Analysis</h5>The detailed chromatographic analyses represent the relative percentages (%) calculated from FID data which are listed in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c07183#tbl1">Table 1</a>. GC-FID and GC/MS analyses of the commercial essential oils verified 20 and 46 compounds, representing 92% and 97.2% of the essential oils, respectively. The main compounds for P. nigra oil were characterized as α-pinene (73.8%), trans-verbenol (4.4%), α-pinene oxide (2%), camphene (1.7%), limonene (1.7%), verbenone (1.6%), and β-pinene, respectively. The main compounds for T. serpyllum were geraniol (19.3%), p-cymene (12.9%), α-thujone (6.6%), linalool (6.4%), carvacrol (5.7%), geranyl acetate (5.6%), geranyl formate (4.3%), and camphor (3.7%), respectively. T. serpyllum and P. nigra essential oil (see Suppl. For Chromatograms in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/suppl/10.1021/acsomega.5c07183/suppl_file/ao5c07183_si_001.pdf">Figure S1 and S2</a>).<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ACS_Omega_2025_10_50_61528_61534_Figure_S1_GCMS_Chromatogram_of_P_nigra_essential_oil_6d0e834f08.jpg" alt="ACS Omega 2025, 10, 50, 61528–61534: Figure S1. GC/MS Chromatogram of P. nigra essential oil" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ACS_Omega_2025_10_50_61528_61534_Figure_S1_GCMS_Chromatogram_of_P_nigra_essential_oil_6d0e834f08.jpg 245w," sizes="100vw" width="1178" height="533"><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ACS_Omega_2025_10_50_61528_61534_Figure_S2_GCMS_Chromatogram_of_T_serpyllum_essential_oil_625414f30d.jpg" alt="ACS Omega 2025, 10, 50, 61528–61534: Figure S2. GC/MS Chromatogram of T. serpyllum essential oil" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ACS_Omega_2025_10_50_61528_61534_Figure_S2_GCMS_Chromatogram_of_T_serpyllum_essential_oil_625414f30d.jpg 245w," sizes="100vw" width="1179" height="503">In a previous study, T. serpyllum essential oil reported 10 different chemotypes, namely: carvacrol, 1,8-cineole/caryophyllene oxide, p-cymene, geraniol, linalool, trans-nerolidol, γ-terpinene, α-terpinol acetate, linalyl acetate, and thymol. <a href="javascript:void(0);">(17−19)</a> Among all, the most common chemotypes of T. serpyllum were suggested as the carvacrol and thymol type. <a href="javascript:void(0);">(3,20)</a> Paaver et al. <a href="javascript:void(0);">(19)</a> observed four chemotypes (trans-nerolidol, caryophyllene oxide, myrcene, and borneol) growing in Estonia. Another study reported that T. serpyllum chemotypes are thymol, caryophyllene oxide, τ-cadinol, β-cubebene, geraniol, geranyl isobutyrate, and 1,8-cineole from Hungary. In this present study, the utilized commercial T. serpyllum essential oil can be classified as geraniol chemotype, in agreement with previous reports in varying concentrations. <a href="javascript:void(0);">(17,21)</a>The major compound of commercial P. nigra essential oil was reported as α-pinene, according to phytochemical analyses. <a href="javascript:void(0);">(22,23)</a>. Regarding the Pinus essential oils in previous reports; α-pinene (44.98%), β-pinene (14.27%), germacrene D (9.63%), limonene (6.93%), and β-caryophyllene (5.58%), respectively was identified in the P. nigra needle oil. <a href="javascript:void(0);">(22)</a> In another study, the main components of pine essential oil were reported as α-pinene (45.93%), germacrene D (27.50%), (E)-caryophyllene (8.13%), and β-pinene (6.90%). <a href="javascript:void(0);">(23)</a>When compared with literature data, the chemical compositions and major compounds showed consistency to previous studies.<h5>2.4. Toxicity Assay</h5>In vitro toxicity tests of the combinations with synergic effects were performed on the HEK293 cell line using the MTT method to evaluate selectivity. According to the FIC values, the combinations of P. nigra-T. serpyllum and P. nigra-amoxicillin were selected for the toxicity evaluation of the essential oils and amoxicillin alone. When the concentrations determined based on the FIC values, all combinations showed higher cell viability compared to the individual MIC values. Based on the data obtained from the cell culture toxicity, a reduction was observed in the combination studies.According to Nikolić et al. <a href="javascript:void(0);">(21)</a> the wild thyme oil, which contains thymol as its major constituent, showed relatively less in vitro cytotoxic activity against four human tumor cells. Deb et al. <a href="javascript:void(0);">(40)</a> reported the T. serpyllum essential oil with antiproliferative activity against HL-60 cells (promyelocytic leukemia).In this present study, designed combinations of commercial essential oils were systematically inhibited the pathogenic microorganism. The utilization of the particular commercially available essential oils, and their combinations with other components for preventing microbial resistance may be applicable.<h4>3. Conclusion</h4>Essential oils with known quality exert new biological and pharmacological activities that carry a utilization potential other than aromatherapy applications. Antimicrobial activity studies using essential oils and their major constituents targeting resistant bacteria may lead to the discovery of new drug leads with potential treatment of various microbial diseases. P. nigra and T. serpyllum oil combinations may have future potential as antimicrobial natural agents. The oil and antibiotic combinations offers a variation enabling relatively higher activity at lower concentrations. Also, combinations of major or minor constituents may not always responsible for synergistic activities, which should be evaluated carefully in depth. The effective combinations may form a basis for future research on upper respiratory tract infections as well as other microbial diseases.However, more detailed studies, including in vivo experiments should be conducted. In addition further research must be performed to explore the use of combinations for the cosmetics and food industries with appropriate design.<h4>4. Material and Methods</h4><h5>4.2. GC/FID and GC/MS Analysis</h5>The GC-MS analysis was carried out with an <a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?mainauthorItems=10&amp;search=5975">Agilent 5975 GC-MSD system</a>. Innowax FSC column (60 m x 0.25 mm, 0.25 μm film thickness) was used with helium as carrier gas (0.8 mL/min). GC oven temperature was kept at 60 °C for 10 min and programmed to 220 °C at a rate of 4 °C/min, and kept constant at 220 °C for 10 min and then programmed to 240 °C at a rate of 1 °C/min. Split ratio was adjusted at 40:1. The injector temperature was set at 250 °C. Mass spectra were recorded at 70 eV. Mass range was from m/z 35 to 450.FID detector temperature was set to 300 °C. To obtain the same elution order with GC-MS, simultaneous autoinjection was applied on a duplicate of the same column applying the same operational conditions. Relative percentage (%) of the separated compounds were calculated from the FID chromatograms.Identification of the essential oil components were carried out by comparison of their relative retention times (RRT) with those of authentic samples or by comparison of their relative retention index (RRI) to series of n-alkanes. Computer matching against commercial (Wiley GC/MS Library, MassFinder Software 4.0) and in-house “Başer Library of Essential Oil Constituents” built up by genuine compounds and components of known oils were performed. <a href="javascript:void(0);">(41)</a></div>

In Vitro Antibacterial Potential of Pinus nigra-Thymus serpyllum Essential Oil and Antibiotic Combinations

<h3><a target="_blank" rel="noopener noreferrer" href="https://www.isc2026.org/">ISC 2026</a></h3>The <a target="_blank" rel="noopener noreferrer" href="https://lcms.labrulez.com/companies/314">International Symposium on Chromatography (ISC)</a> represents the oldest conference series on separation science. ISC symposia have been organised since 1956 in each even year. ISC is one of the premier meetings series for discussion of all modes of chromatography and separation science with a broad coverage of techniques and applications.The major focus of the symposium will be on the impact of chromatography and separation science to meet the needs of the pharmaceutical, environmental, food and health industry, as well as science and medicine. The symposium programme will reflect these themes and highlight new challenges and emerging opportunities for the science and marketing of separation and detection systems and methods.As an integral part of the scientific programme of lectures and poster sessions, an international exhibition and vendor seminars on instrumentation and services for chromatography, separation science and mass spectrometry will be organised. ISC 2026 will provide the perfect forum for attendees from academia, industry and government research institutions for scientific exchange and networking.<h3>ISC 2026 SYMPOSIUM KEY DATES</h3><h4>6-10 SEPTEMBER 2026</h4><ul><li>15 January 2026: Opening of Early-bird Registration &amp; Abstract submission</li><li>11 March 2026: Deadline for abstract submission (orals)</li><li>21 April 2026: Sending acceptance letters (orals)</li><li>15 May 2026: Deadline of early-bird registration and payment &amp; Author registration deadline (orals)</li><li>1 June 2026: Preliminary detailed program on web</li><li>1 June 2026: Deadline for abstract submission (posters)</li><li>16 June 2026: Sending acceptance letters (posters)<ul><li>Authors who submit their abstracts with a poster preference by 5 May 2026 will be notified of the outcome by 12 May 2026 and will have the opportunity to register at the early-bird rate until 15 May 2026.</li></ul></li><li>30 June 2026: Author registration deadline (posters)</li><li>30 July 2026: Deadline for abstract submission (late-breaking posters)<ul><li>without the possibility of competing for the Best Poster Award</li></ul></li><li>11 August 2026: Sending acceptance letters (late-breaking posters)</li><li>18 August 2026: Author registration deadline (late-breaking posters)</li><li>25 August 2026: Deadline for late registration &amp; payment&nbsp;</li><li>6-10 September 2026: Symposium</li></ul><h3>REGISTRATION</h3><blockquote>👉<a target="_blank" rel="noopener noreferrer" href="https://www.czech-in.org/cmPortalV15/Account/Login?ReturnUrl=%2FcmPortalV15%2FPortal%2FISC26%2Fnormal">Register HERE for the ISC 2026</a></blockquote><h3>ABSTRACT SUBMISSION</h3><blockquote>👉<a target="_blank" rel="noopener noreferrer" href="https://www.czech-in.org/cmPortalV15/Account/Login?ReturnUrl=%2FcmPortalV15%2FPortal%2FISC26%2Fnormal">Submit your Abstract HERE</a></blockquote><h3>SCIENTIFIC PROGRAM</h3><h4>SHORT COURSES</h4><h5>SC 5 Oligonucleotides and Other Biopharmaceuticals</h5>🗓️ SUNDAY, 6 SEPTEMBER 2026🕗 12:30 – 15:45Analysis of nucleic acid and protein-based pharmaceuticalsThe pharmaceutical industry has undergone a profound transformation over the past four decades driven by continuous innovation in therapeutic and prophylactic modalities. While small molecules have been the foundation of medicine for ages, successive waves have introduced biologics such as recombinant proteins and antibodies, in addition to nucleic acid and cell-based products. Each wave has expanded our ability to treat diseases but also challenged us, analytical scientists, to build a toolbox to characterize these ever more complex modalities. This short course will cover chromatographic and mass spectrometric methods for analyzing nucleic acid and protein-based medicines including antisense oligonucleotides (ASOs), small interfering ribonucleic acid (siRNA) and larger nucleic acids such as messenger RNA (mRNA), in addition to monoclonal antibodies (mAbs), antibody-drug conjugates (ADCs) and &nbsp;antibody-oligonucleotide conjugates (AOCs).&nbsp;<h4>Lecturers</h4><h5>Koen Sandra</h5><ul><li>Koen Sandra received a PhD degree in Biochemistry from the Ghent University, Belgium in 2005. After his PhD, he joined Pronota, a molecular diagnostics company where he was active in developing analytical platforms for disease biomarker discovery and in setting up external collaborations. In 2008, he joined RIC, a company that provides analytical support to the chemical, life sciences and pharmaceutical industries, where he holds the position of CEO. As a non-academic scientist, Koen Sandra is author of over 50 highly cited scientific papers and has presented his work at numerous conferences as an invited speaker.</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ISC_2026_Koen_Sandra_2ff9f97b34.jpg" alt="ISC 2026: Koen Sandra" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ISC_2026_Koen_Sandra_2ff9f97b34.jpg 156w," sizes="100vw" width="500" height="500"><h5>Amanda Guiraldelli Mahr</h5><ul><li>Amanda Guiraldelli Mahr is a senior scientist at the RIC group in Belgium, specialized in chromatographic and LC-MS strategies for biopharmaceutical and small molecule analysis. With more than 17 years of experience in analytical development, she leads the design and qualification of procedures for release testing, stability studies, and structural characterization of monoclonal antibodies, peptides, and oligonucleotides, with strong expertise in SEC, IEX, RPLC, HILIC, HIC, and high-resolution MS workflows. She drives the implementation of ICH Q2(R2), Q14, and Analytical Quality by Design (AQbD) principles in collaboration with global biopharmaceutical partners. Amanda serves as a member of the United States Pharmacopeia (USP) Pharmaceutical Analytical Lifecycle and Data Science Expert Committee and is a board member of the ECA Analytical Quality Control Group. Before joining RIC, she spent more than 12 years at USP, where she worked both as a Senior Scientist – leading method development and validation projects, impurity analysis by LC-MS/GC-MS, and reference standards characterization by LC-HRMS – and as a Scientific Affairs Manager, contributing to major standards such as &lt;1220&gt; and &lt;1225&gt; and driving initiatives in AQbD, predictive modeling, and analytical procedure lifecycle management. She holds a bachelor’s degree in Pharmacy–Biochemistry and a Ph.D. in Analytical Chemistry, and has been a visiting scientist at TU Berlin and Leiden University, focusing on LC-HRMS-based protein analysis.</li></ul><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ISC_2026_Amanda_Guiraldelli_Mahr_0bd046c778.jpg" alt="ISC 2026: Amanda Guiraldelli Mahr" srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ISC_2026_Amanda_Guiraldelli_Mahr_0bd046c778.jpg 156w," sizes="100vw" width="500" height="500">

ISC 2026 Short Course 5 - Oligonucleotides and Other Biopharmaceuticals

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LabRulez

The International Symposium on Chromatography (ISC) represents the oldest conference series focussing on separation science. ISC symposia have been organised since 1956 in each even year. ISC is internationally recognised as one of the premier meeting series for discussion of all modes of chromatography and separation science with a broad coverage of techniques and applications.

International Symposium on Chromatography - (ISC)

CEM Corporation

Separation Science

ACD/Labs

SepSolve Analytical

Thermo Fisher Scientific

Quantum Analytics

SelectScience

Session 1: Learn how automation can simplify the analysis in your lab utilizing RSH SMART technology. Make your results safer and less cost intensive.
Session 2: The future in GC-MS/MS analysis. New technologies to overcome old but very well-known issues in the analysis of pesticides. Learn how to improve your results from experienced people.
Session 3: Ethylene oxide 2.0 stands for issues that are not yet solved, such as false positive results for ethylene oxide and 2-chloroethanol. This webinar will show relevant data on different matrices.
<h3>Who should attend:</h3>
<ul>
<li>Lab managers and analysts that have analytical challenges when testing food and beverages</li>
<li>QA/QC and research laboratories that want to keep up to date and also be ready for future challenges</li>
<li>Lab leaders who want to leverage the full analytical potential of their analytical instrumentation</li>
</ul>
<blockquote>
Presenter: Petra Gerhards (Regional Marketing Manager EMEA GC, GC-MS, Thermo Fisher Scientific)
</blockquote>
<blockquote>
Her background is over 30 years of experience in the field of GCMS, SPE and LCMS. Joined the EMEA Regional Marketing Team in 2016. She has been involved in a lot of workflow solutions combining Vials and Closures with SPE solutions, GCMS and LCMS. She works with KOL`s on data for regional specific marketing campaigns, organizes inhouse seminars and works on customer specific solutions. Her main expertise is in the field of Doping and Drugs of Abuse analysis.
</blockquote>

Thermo Fisher Scientific: Emerging Topics in Food Safety

Pesticide residues analysis by GC-MS

Automation utilizing RSH SMART technology, The future in GC-MS/MS analysis and will show relevant data on different matrices for Ethylene oxide analysis.

It’s time to take your engineering experiments to the next level with the power of real-time. When monitoring vapor phase streams from experiments and reactors, speed of analysis is critical. To offer true real-time analysis, data acquisition and display rates must be on a second-based timeframe. This eliminates many of the common analytical techniques for gas monitoring, which are also limited in scope to only a portion of the sample. Fortunately, Mass Spectrometry (MS) is broad in analytical capability to include the entire sample, and it can be very fast.
Join us for a webinar where we’ll look in detail at the requirements of MS for real-time analysis. But more importantly, the requirements will be covered for quantitative results. Often, MS for gas analysis is practiced as only a “trend monitoring” tool. However, MS can be designed and implemented for quantitative experiments with gas streams. Under proper interface design, calibrations can be linear, reliable, and easy to establish with common external standard calibrations.
The systems presented in this webinar will emphasize Engineering and Research experiments in laboratories, mini-hoods, experimental reactors, and other development phase experiments. We’ll discuss system robustness and critical interface designs that eliminate common pressure problems and matrix effects from most gas streams. This webinar will not address on-line production systems; however, the principles would apply for gas analysis by MS in general.
<h3>Key Webinar Topics:</h3>
<ul>
<li>Fast analysis of gas streams</li>
<li>Quantitative gas analysis by MS</li>
<li>Full sample analysis while addressing the matrix</li>
</ul>
<blockquote>
Presenter: Terry Ramus, PhD (Principal, Diablo Analytical)
</blockquote>
<blockquote>
Over the last 35 years, Dr. Terry Ramus has done research in gas phase analytical techniques with an emphasis on applications of Mass Spectrometry and GC/MS for the industrial and engineering sectors. Application areas include process measurements for Engineering experiments such as catalysis, reactor performance, yield optimization, and scale-up. Experiments include alternative energy, syngas, and pyrolysis. These experiments include hardware and software for analytical systems, including mass spectrometry, chromatography, and other spectroscopic and discrete analytical techniques. For over 20 years now, research has emphasized the characterization of process gases in Real-time with Real-time Mass Spectrometry (RTGA-MS). Other efforts are centered on Pyrolysis-GC/MS for polymer and material characterization characterization and deformulation. During these years, Dr. Ramus has worked as a Principal with Diablo Analytical, Inc. from his laboratory in California. Dr. Ramus received his Ph.D. in Analytical Chemistry from Oregon State University in 1985.
</blockquote>
<blockquote>
Presenter: Scott Hein, PhD (Principal, Diablo Analytical)
</blockquote>
<blockquote>
Dr. Scott Hein is a principal of Diablo Analytical, a technology and development company.
</blockquote>

Quantum Analytics: Gas Analysis in Real-Time by MS

Gas Analysis in Real-Time by MS

It’s time to take your engineering experiments to the next level with the power of “real-time”. Discover gas analysis in real-time by mass spectrometry. 

We’re very excited to bring you a 6 part series of webinars that will air on Wednesdays beginning March 23 and concluding April 6. Each Wednesday there will be a 1 hour webinar from 11:00AM – 12:00PM (EST) and a 1 hour webinar from 3:00PM to 4:00PM (EST) on a range of different applications and topics using the miniGC, miniGAS and miniLC featuring:
<ul>
<li>Dr. Ronda Gras of Dow Chemical</li>
<li>Prof. Jim Grinias of Rowan University</li>
<li>Prof. Emanuela Gionfriddo of The University of Toledo</li>
<li>Todd Griffin of G2 Analytical</li>
<li>Prof. Nick Snow of Seton Hall University</li>
<li>Dr. Alicia Stell of CEM Corporation/Lucidity</li>
</ul>
CEM | Lucidity is pleased to bring together leaders in the field of chromatographic separation to highlight their cutting edge research and share their techniques with the scientific community. Join us each Wednesday to learn about what is new in chromatography and have the opportunity to ask questions after each talk.
<h3>Wed April 6</h3>
<h4>5:00 – 6:00 PM Utilizing Compact, Integrated Chromatographic Instrumentation for Pharmaceutical Analysis</h4>
In the realm of quality assurance and quality control within the pharmaceutical industry, reliable and robust analytical methodology is of utmost importance. Many pharmaceutical analysis techniques rely upon chemical separations, especially the use of LC-UV for drug substance and impurity assays. In this presentation, considerations for method development, method validation, and system suitability will be explored in the context of small molecule pharmaceutical analysis, especially common over-the-counter analgesic compounds with published pharmacopeial monograph methods. Considerations for acceptable changes that can be made to methods within pharmacopeial guidelines will also be discussed, including potential advantages and disadvantages that may be observed for various changes. Finally, multiple examples of analgesic drug analysis performed using the new miniLC platform will be demonstrated.
<blockquote>
Presenter: Alicia D. Stell, PhD (Product Manager, Organic Solutions Division, CEM Corporation)
</blockquote>
<blockquote>
Dr. Alicia Douglas Stell has worked with CEM for the past 14 years joining after completing her PhD in Analytical Chemistry. Her extensive background in chromatographic analysis and her mechanical expertise have been instrumental in the development of novel systems for sample preparation and analysis. She has traveled the world to present on these novel systems and to identify new markets for this innovative technology.
</blockquote>
<blockquote>
Presenter: James P. Grinias (Associate Professor, Department of Chemistry &amp; Biochemistry, Rowan University)
</blockquote>
<blockquote>
James Grinias is currently an Associate Professor in the Department of Chemistry &amp; Biochemistry at Rowan University in Glassboro, NJ. His research interests include improving the throughput and efficiency of chromatographic separations and the miniaturization of chemical measurement techniques. He received his Ph.D. from the University of North Carolina at Chapel Hill in 2014 and the moved onto a postdoctoral fellowship at the University of Michigan until the end of 2016. James has received a number of awards for his work to date, including the HPLC 2013 Csaba Horváth Award, the 2020 Young Investigator Award from the Chinese American Chromatography Association, a National Science Foundation CAREER grant, the 2021 American Chemical Society Satinder Ahuja Young Investigator in Separation Science Award, and the 2022 LCGC Emerging Leader in Chromatography Award. He was also named to The Analytical Scientist’s “Top 40 Under 40” Power List in 2018. To date, he has published over 30 articles and given over 80 oral/poster presentations.
</blockquote>
<h4>9:00 – 10:00 PM Training the next generation of chromatographers using Lucidity miniGC in the research and teaching laboratories</h4>
This webinar will describe applications of the Lucidity miniGC for research and teaching purposes. Research projects describing analysis of plant volatiles and determination of residual solvents in recycled acetone will be discussed, as well various strategies to implement the use of the miniGC in the analytical chemistry laboratories and provide the students with hands-on experience on a user-friendly chromatographic system.
<blockquote>
Presenter: Emanuela Gionfriddo, PhD (Assistant Professor, Department of Chemistry and Biochemistry, The University of Toledo)
</blockquote>
<blockquote>
Dr. Emanuela Gionfriddo is an Assistant Professor of Chemistry at the Department of Chemistry and Biochemistry of The University of Toledo (OH, USA). Research work in Dr. Gionfriddo’s lab focuses on developing advanced analytical separation tools for the analysis of complex biological and environmental samples using alternative green extraction methodologies. She received her Ph.D. in Analytical Chemistry (2013) at the University of Calabria (Italy). She joined Prof. Pawliszyn’s group at the University of Waterloo (Ontario, Canada) in 2014 as a Post-Doctoral Fellow and manager of the Gas-Chromatography section of the Industrially Focused Analytical Research Laboratory (InFAReL), and within three years became a Research Associate. Dr. Gionfriddo has currently authored over 50 peer-reviewed contributions including a patent on PTFE-based SPME coatings. Dr. Gionfriddo is one of the founding members of the Dr. Nina McClelland Laboratory for Water Chemistry and Environmental Analysis at The University of Toledo and she is appointed to the Ohio Attorney General Yost’s Environmental Council of Advisors. She also serves as the secretary of the ACS Subdivision on Chromatography and Separations Chemistry. Her research program is currently funded by the National Science Foundation through the 2022 CAREER Award, by the National Oceanic and Atmospheric Administration and several industrial partnerships.
</blockquote>
<blockquote>
Presenter: Alicia D. Stell, PhD (Product Manager, Organic Solutions Division, CEM Corporation)
</blockquote>
<blockquote>
Dr. Alicia Douglas Stell has worked with CEM for the past 14 years joining after completing her PhD in Analytical Chemistry. Her extensive background in chromatographic analysis and her mechanical expertise have been instrumental in the development of novel systems for sample preparation and analysis. She has traveled the world to present on these novel systems and to identify new markets for this innovative technology.
</blockquote>

CEM/Lucidity: Wednesday Webinars on Separation Solutions

Wednesday Webinars on Separation Solutions

Utilizing Compact, Integrated Chromatographic Instrumentation for Pharma. Training the next generation of chromatographers using Lucidity miniGC.

With the food industry subject to increasing scrutiny, comprehensive testing solutions are required to determine the authenticity and contaminant-free status of food products and to ensure their compliance with safety regulations.
In this SelectScience® roundtable webinar series, we bring together leading experts in the fields of pesticides analysis, mycotoxin testing and food contact materials characterization to discuss the latest trends in these areas and laboratory innovations set to transform the future of food safety testing. This series consists of three panel discussions, starting on Wednesday, March 23rd.
<h4>Webinar 1: Modernizing pesticides testing</h4>
Wednesday, March 23, at 16:00 GMT / 17:00 CET / 12:00 EDT / 09:00 PDT
<h4>Webinar 2: Measuring migration from food contact materials</h4>
Thursday, April 7th, at 16:00 BST / 17:00 CEST / 11:00 EDT / 08:00 PDT
<h4>Webinar 3: Identifying and controlling mycotoxins in livestock and food products</h4>
Tuesday, April 12th at 16:00 BST / 17:00 CEST / 11:00 EDT / 08:00 PDT
<blockquote>
Presenter: Susanne Ekroth (Chemist, National Food Agency EU)
</blockquote>
<blockquote>
Susanne Ekroth is an analytical chemist at the Swedish National Food Agency. She graduated from Uppsala University and has been working at the Swedish National Food Agency for 27 years as a pesticide expert. During this time, she has developed skills in advanced technology, including GC-MS/MS, LC-MS/MS and LC-HRMS and is one of the founders of the multi residue method SweEt. Besides pesticides, she also works with food contact materials and toxins in water. 
</blockquote>
<blockquote>
In recent years, Susanne has focused on HRMS techniques and the possibility to replace the LC-triple quadrupoles with LC-MS Orbitrap and simultaneously screen for new and unwanted compounds in food matrices. This work is presented as an application note and webinar as well as in Food Safety Magazine.
</blockquote>
<blockquote>
Susanne is a member of the Scientific Organizing Committee for EPRW (European Pesticide Residue Workshop) and IUPAC (Pesticide Congress, Food Quality and Safety). She has given presentations about her work on the SweEt multiresidue method on several occasions, for example at the Nordic-, European- and Latin American Pesticide Residue Workshop, RAFA and Fresenius.
</blockquote>
<blockquote>
Climate change and adaptation have become one of the world&#39;s most important issues and have in recent years become increasingly integrated into the authorities&#39; work. How it can affect lab work and the planning of the official controls are some of the issues that Susanne has been working on in recent years. Working with climate and vulnerability analyses and action plans is under governmental regulation, but it also enables us to be prepared for new substances and new types of food in our screening methods. This type of methodology is very familiar to the pesticide community and future adaptions should work very well. Susanne will present some of the upcoming needs due to climate change.
</blockquote>
<blockquote>
Presenter: Steven Lehotay (Lead Scientist, USDA-ARS)
</blockquote>
<blockquote>
Steven J. Lehotay is a Lead Scientist with the USDA Agricultural Research Service at the Eastern Regional Research Center in Wyndmoor, Pennsylvania. Since 1992, he has conducted scientific investigations and method development research involving improvement in the analysis of pesticides, veterinary drugs, and other contaminants in food and environmental samples. He is the co-inventor of the “quick, easy, cheap, effective, rugged, and safe” (QuEChERS) sample preparation approach. He has been awarded with numerous honors, including the AOAC International Harvey W. Wiley Award, and according to the Stanford c-score metric, he resides among the top 0.19% of published analytical chemists.
</blockquote>
<blockquote>
Presenter: Dr. Jim Garvey (Head of Food Chemistry, Department of Agriculture, Food and the Marine, Ireland)
</blockquote>
<blockquote>
Dr. Jim Garvey graduated from The National University of Ireland (Galway) in 1988 with a Ph.D. in Organic Chemistry. After seven years in the pharmaceutical industry as a Research Chemist, he became the process development manager in a company producing high purity solvents for GC, HPLC, and MS. He joined the Pesticide Control Laboratory in 1999 and led the laboratory through many changes -- from the introduction of mass spectrometry techniques through various phases culminating in the implementation of HRMS techniques. He led the laboratory through the 2008 dioxin crisis. Since then he has overseen many phases of laboratory development and is currently managing the introduction of HRAM technology to the residues laboratory. In October 2019, he was appointed Head of Food Chemistry at the Department of Agriculture, Food and the Marine. As well as pesticides, the Food Chemistry division covers veterinary drugs, compositional analysis of dairy products, contaminants and elemental analysis. The objective of the new division is to build a centre of excellence for food chemistry within the Department of Agriculture Food and the Marine.
</blockquote>
<blockquote>
Presenter: Jana Hajšlová (Head of the Department of Food Analysis and Nutrition, UCT Prague)
</blockquote>
<blockquote>
Professor Jana Hajšlová is Head of the Department of Food Chemistry and Analysis at the Institute of Chemical Technology, Prague. Since 2000, she has been Head of Accredited Laboratory (ISO 17025) focusing on the analysis of food and environmental contaminants, toxicants and biologically active compounds.
</blockquote>
<blockquote>
Presenter: Dr. Yelena Sapozhnikova (Research Chemist, USDA-ARS)
</blockquote>
<blockquote>
Dr. Yelena Sapozhnikova is a Research Chemist at the Agricultural Research Service, United States Department of Agriculture (USDA) in Wyndmoor, PA, USA. Her research focuses on the development of new methods for the residual analysis of chemical contaminants, including pesticides, environmental and emerging contaminants, food packaging chemicals using gas and liquid chromatography with mass spectrometry. Dr. Sapozhnikova has over 20 years of experience in the analysis of chemical contaminants in food and environmental samples.
</blockquote>
<blockquote>
Presenter: Cristina Nerín (Professor of Analytical Chemistry, University of Zaragoza)
</blockquote>
<blockquote>
Dr. Cristina Nerín is Professor of Analytical Chemistry at the University of Zaragoza, Spain. She is the Director of the Research Group GUIA at the University of Zaragoza and was Director of the Master in Environmental Engineering program from 1990 to 2012. Dr. Nerín is an author of more than 320 scientific publications. Dr. Nerín is also Principal Investigator of more than 200 research projects and an inventor in eight international Patents related to packaging, all in commercial applications. Dr. Nerín has received six research awards, participated in more than 140 international conferences, and instructed courses in Europe, Asia and South-America. Dr. Nerín is on the organizing committee and Chair of several international symposia.
</blockquote>
<blockquote>
Presenter: Dwayne Shrunk (Laboratory Manger of Analytical Chemistry Services, Veterinary Diagnostic Laboratory (VDL) at Iowa State University)
</blockquote>
<blockquote>
Dwayne is an accomplished analytical chemist with over 25 years of laboratory experience both as an operator and manager. While supporting research and collaborative partnerships, he is well versed in method development and validation, QA/QC, and lab information management. VDL is recognized as national leader in protecting animal and human health, Wayne’s leadership at one of the full-service laboratories at the VDL process upwards of 100,000 cases each year and conduct more than a million tests annually. As a fully accredited facility by the American Association of Veterinary Laboratory Diagnosticians, the VDL provides quality diagnostic services for animal species, including necropsy, bacteriology, serology, histopathology, virology, parasitology, molecular diagnostics, and toxicology as well as offering analytical services, where understanding the impact natural toxins contribute to the ongoing health of animals is important.
</blockquote>
<blockquote>
Presenter: Tim Stratton (Manager of Library Technologies, Thermo Fisher Scientific)
</blockquote>
<blockquote>
Graduate of the University of Minnesota. Started my career as an analyst in pharma working in regulated analysis, quality control, method validation, etc. for many years with Solvay Pharmaceuticals. Migrated into pharma research when I moved to Abbott Laboratories working in drug metabolism and pharmacokinetics in all aspects from early high throughput screening to post market phase 4 studies. My work in research extended for almost 10 years and included working for both large and small pharma companies. My specific area of focus was structure elucidation and fragmentation interpretation and it’s still an area I really enjoy. I joined Thermo Fisher almost ten years ago working in the Pharma vertical marketing group, mainly because they promised I could play with the latest toys before they were available. Since then I’ve been involved in hardware and software testing and development as well as working directly with customers for support and to better understand their needs. The past few years I’ve transitioned to focus more on the construction of high resolution accurate mass MS/MS and MSn spectral libraries to help with identification of unknowns across all areas of research and this continues to be the main area of focus for me.
</blockquote>

SelectScience: Emerging trends and future directions in food testing

Measuring migration from food contact materials (Emerging trends and future directions in food testing)

In this webinar series, we bring together leading experts in the fields of pesticides analysis, mycotoxin testing and food contact materials characterization.

Measuring migration from food contact materials

This virtual forum will discuss the risk assessment and analytical challenges of detection and quantification of trace level impurities in pharmaceutical products including mutagenic nitrosamine impurities, other mutagenic impurities and will also consider what’s next. With expert leaders in impurity profiling strategies and trace analysis we will discuss the risk assessment of mutagenic impurities and the difficulties in analysis from sample preparation through to detection.
The importance of sample preparation and matrix effects and how automation may help will be discussed as well as how best to avoid false positives. The different technologies available for trace level analysis will be considered as well as the difficulties in technology transfer.
<h3>By attending this webinar you will learn:</h3>
<ul>
<li>What are impurities and where do they come from</li>
<li>Risk analysis, nitrosamine sources and specification setting</li>
<li>Regulatory and compendial perspectives</li>
<li>Alleviating the risk of impurity formation by better understanding of the active pharmaceutical ingredients, its source and manufacturing process.</li>
<li>Difficulties in sample preparation, what to do and not to do</li>
<li>The use of automation in trace level impurity analysis</li>
<li>How to avoid false positives and consideration of matrix effects</li>
<li>The different types of technologies available for trace impurity analysis</li>
<li>New detector technology including vacuum UV and nitrogen Phosphorus detectors</li>
<li>Minimising the risk in technology transfer</li>
<li>Unmet analytical needs</li>
</ul>
<blockquote>
Presenter: Adrian Clarke (Global Technical R&amp;D Analytical Network Leader, Novartis)
</blockquote>
<blockquote>
Presenter: Jörg Schlingemann (Principal Expert Quality Control Systems at EMD Serono)
</blockquote>
<blockquote>
Presenter: Tony Bristow (Principal Scientist for Measurement Science, AstraZeneca)
</blockquote>
<blockquote>
Presenter: Naiffer Romero (Sr Manager, Scientific Affairs, LATAM, US Pharmacopeia)
</blockquote>
<blockquote>
Presenter: Amanda Guiraldelli Mahr (Scientific Affairs Manager, US Pharmacopeia)
</blockquote>

Unsplash/Raimond Klavins: Detection and Quantification Challenges of Trace Level Impurities in Pharmaceutical Products - Mutagenic Nitrosamines and Beyond

Detection and Quantification Challenges of Trace Level Impurities in Pharmaceutical Products - Mutagenic Nitrosamines and Beyond

Pharmaceutical Products - Mutagenic Nitrosamines and Beyond

Wires tangle behind lab benches and instruments, WIFI signals travel through the air. Transferring data all day every day. Your lab is a digital lab!
Perhaps due to its diversity and volume, or because scientists find it difficult to map to business objectives, analytical data is rarely a priority in digitalization projects.
In this webinar series we will help you make analytical data part of your digital transformation journey. Forget the buzz words and focus on what you need and how to accomplish it.
In this first webinar of the series, we will share practical strategies for the digital transformation of analytical data.
<h5>When is the right time?</h5>
Are you waiting to make decisions about standardizing your data or aligning various workflows or processes?
<h5>Where do you start?</h5>
Analytical data supports numerous processes and workflows from discovery through manufacturing. How do you tackle digitalization of this diverse, high volume data that is used is so many different ways?
<h5>Is cloud the answer?</h5>
IT teams are pushing for data to move to the cloud where it&#39;s accessible and space is &quot;unlimited&quot;. Are there any downsides you need to consider?
Join us as we discuss these questions and more so you can align your analytical data digitalization aspirations with business goals and IT&#39;s objectives.
<h3>Who should attend?</h3>
<ul>
<li>Scientists - you manage analytical instruments/are interested in how analytical instrument are set up and maintained/analytical data is critical to your work</li>
<li>IT Whisperers - you liaise between scientific groups and IT teams when choosing software or defining requirements</li>
<li>Data Scientists - you&#39;re interested in how analytical data can benefit from &#39;Big Data&#39;, &#39;the cloud&#39;, and &#39;machine learning&#39;</li>
</ul>
<blockquote>
Presenter: Andrew Anderson (Vice President Innovation &amp; Informatics Strategy, ACD/Labs)
</blockquote>
<blockquote>
Host: Sanji Bhal (Director, Marketing &amp; Communications, ACD/Labs)
</blockquote>

ACD/Labs: Digitalization & Analytical Data

Digitalization of Analytical Workflows: Strategies for Success

In this first webinar of the series, we will share practical strategies for the digital transformation of analytical data.

Digitalization of Analytical Workflows: Strategies

Problems can arise from any component in your gas chromatography (GC) setup. In order to troubleshoot and solve these issues quickly and efficiently, it is important to follow systematic processes.
In this webinar, Dr. Ramkumar Dhandapani, global product manager of gas chromatography at Phenomenex, will walk you through a systematic approach to identify, resolve, and prevent GC-related problems. In addition, diagnostic approaches will be explored for solving issues in GC analysis. Troubleshooting with specific case studies including the analysis of volatiles, semivolatiles, and persistent organic pollutants (POPs) will also be explored.
<h3>Key learning objectives</h3>
<ul>
<li>Understand the basic concepts of GC</li>
<li>Discover systematic ways to troubleshoot complex problems</li>
<li>How to choose the right GC column for your application</li>
<li>Strategic troubleshooting for persistent organic pollutants with case studies</li>
</ul>
<h3>Who should attend?</h3>
<ul>
<li>Analytical chemists that need help with GC troubleshooting</li>
<li>Academic researchers that require strategic troubleshooting tips</li>
<li>GC lab managers that want to reduce lab downtime</li>
</ul>
<blockquote>
Presenter: Dr. Ramkumar Dhandapani (Global Product Manager - Gas Chromatography, Phenomenex)
</blockquote>
<blockquote>
Dr. Ramkumar Dhandapani has been in the chromatography industry for over 18 years with hands-on and troubleshooting experience. He has earnt a master’s and Ph.D. degree in analytical chemistry from Seton Hall University, with specializations in microextractions, multidimentional gas chromatography, and tandem mass spectroscopy techniques. He has developed and validated several regulatory compliant methods in the pharmaceutical, food, fuels and environmental industries as well as incorporated method improvement and troubleshooting across a range of separation techniques. Dr. Dhandapani joined Phenomenex in August of 2014 and he serves as the global product manager of gas chromatography. In addition to managing the GC product line, Dr. Dhandapani presents on innovations in GC at various chromatography conferences.
</blockquote>
<blockquote>
Presenter: Blake Forman (Editorial Team, SelectScience)
</blockquote>
<blockquote>
Blake studied chemistry at the University of Surrey, UK, and further went on to study a master’s in chemistry at the University of Southampton, UK. Blake has previously worked in the Medicines and Healthcare Products Regulatory Agency (MHRA) lab at LGC and as a technical sales specialist for Waters. As a member of the Editorial team, he now plays an integral role in shaping the content on SelectScience.
</blockquote>

SelectScience: GC troubleshooting tips and tricks from inlet through to detection

GC troubleshooting tips and tricks from inlet through to detection

In this webinar, Dr. Ramkumar Dhandapani, will walk you through a systematic approach to identify, resolve, and prevent GC-related problems.

GC troubleshooting tips and tricks from inlet to detection

Do you struggle to get reliable answers from your MS data?
Join us for this webinar to see how BenchTOF2 time-of-flight mass spectrometers can be integrated into discovery and routine workflows to fulfil your rapid return on investment goals.
At SepSolve, we provide the most powerful analytical solutions with the know-how to help you get the most from your work, whatever the application. Using our ChromSpace® software suite, we will show how you can make the most of your data and quickly generate meaningful results across a range of GC–MS applications.

SepSolve: End-to-end workflows to solve problems in separation science

End-to-end workflows to solve problems in separation science

Do you struggle to get reliable answers from your MS data? Join us to see how BenchTOF2 MS can be integrated into discovery and routine workflows

Are you sure you always identify your compounds correctly?
Do you want to benefit from hard and soft ionisation without any compromise?
Tune in to this webinar to hear what Tandem Ionisation by BenchTOF2 time-of-flight mass spectrometers can do for you. 
Our patented Select-eV ion source provides an extra dimension of insight into sample composition, by providing both hard and soft ionisation simultaneously. The complementary spectra offer unique confidence in identification with no added analysis time.

SepSolve: How to benefit from soft ionisation without compromise

How to benefit from soft ionisation without compromise

Tune in to this webinar to hear what Tandem Ionisation by BenchTOF2 time-of-flight mass spectrometers can do for you. 

Have you ever wondered how you can get reference quality spectra from a time-of-flight MS?
Join us for this webinar to hear how BenchTOF instruments provide unparalleled spectral quality, improved mass accuracy and accurate isotope abundances – removing the guesswork and complexity commonly associated with analyte identification.

SepSolve: How to improve confidence in your GC–MS identifications

How to improve confidence in your GC–MS identifications

How BenchTOF instruments provide unparalleled spectral quality, improved mass accuracy and accurate isotope abundances.

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