This study investigates the chemical transformations of Eugenia uniflora essential oil under thermal conditions simulating gas chromatography analysis. GC–MS and NMR revealed that sesquiterpenes of the germacrene type, such as furanodiene, undergo sigmatropic rearrangement to form elemene-type compounds, including curzerene.Thermal treatment confirmed the formation of rearrangement products, indicating that bioactive properties historically attributed to curzerene may instead originate from furanodiene. The findings highlight the importance of combining complementary analytical techniques, such as NMR, to avoid misinterpretation of essential oil composition and bioactivity markers.<blockquote><h4>The original article</h4><h4><a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c08966">Is Curzerene Responsible for the Bioactive Properties of Eugenia uniflora? A Possible Misinterpretation of Bioactive Markers</a></h4>Vinicius Monteiro Schaffka, Raphaela Pereira Guaringue, Larissa Kozan, André Luis Kerek, Cássia Gonçalves Magalhães, Andersson Barison, and Barbara Celânia Fiorin*ACS Omega 2025, 10, 48, 59425–59434<a target="_blank" rel="noopener noreferrer" href="https://doi.org/10.1021/acsomega.5c08966">https://doi.org/10.1021/acsomega.5c08966</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>Essential oils are a matrix of volatile and complex compounds characterized by strong odors and significant biological activity. In plants, they play a crucial role in defense against bacteria, viruses, and predators. <a href="javascript:void(0);">(1)</a> These biological properties support the extensive use of essential oils in the food, cosmetics, and pharmaceutical industries. <a href="javascript:void(0);">(1,2)</a> Eugenia uniflora L., commonly known as pitangueira, is a native Brazilian tree widely distributed across South America and is well-known for its bioactive essential oil. <a href="javascript:void(0);">(3)</a> Beyond the consumption of its fruits in natura or functional beverages, its leaves are used in infusions, decoctions, and tinctures to treat a variety of diseases, including diarrhea, stomach pain, worm infestations, fever, flu, hyperglycemia, hyperlipidemia, and hypertension. <a href="javascript:void(0);">(4,5)</a> Studies have shown that the composition of secondary metabolites in E. uniflora can vary depending on factors such as fruit color, ripening stage, <a href="javascript:void(0);">(6)</a> and seasonal influences. <a href="javascript:void(0);">(4,7−10)</a>The essential oil of E. uniflora is predominantly composed of sesquiterpenes, mainly germacrene-type, such as curzerene, germacrene B, germacrone, germacrene D, selina-1,3,7(11)-trien-8-one, and its oxide. Additionally, Elemene-type terpenes are also reported, including furanodiene, β-Elemene, and β-Elemenone. <a href="javascript:void(0);">(11−13)</a>However, those sesquiterpenes are well-documented for their thermal instability. When heat is applied, germacrene-type sesquiterpenes undergo a [3,3]-sigmatropic rearrangement, known as Cope rearrangement, converting into Elemene-type terpenes as presented in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c08966#fig1">Figure 1</a>. <a href="javascript:void(0);">(14−16)</a> This reaction is widely utilized as a synthetic pathway to produce Elemenes from germacrene precursors. <a href="javascript:void(0);">(17,18)</a><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ACS_Omega_2025_10_48_59425_59434_Figure_1_3_3_Sigmatropic_rearrangement_of_Germacrene_type_into_Elemene_type_250708e73c.jpg" alt="ACS Omega 2025, 10, 48, 59425–59434: Figure 1. [3,3]-Sigmatropic rearrangement of Germacrene-type into Elemene-type." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ACS_Omega_2025_10_48_59425_59434_Figure_1_3_3_Sigmatropic_rearrangement_of_Germacrene_type_into_Elemene_type_250708e73c.jpg 245w," sizes="100vw" width="3000" height="984">Gas chromatography (GC) is the main technique for characterizing essential oils, often coupled with mass spectrometry (GC-MS) and the retention index determination is used in the identification of the compounds through comparison with databases. <a href="javascript:void(0);">(21)</a> During GC analysis, essential oils are subjected to multiple heating stages. Initially, the sample is exposed to a high inlet temperature, typically around 240 °C, to ensure complete volatilization. It then enters the oven, where the temperature follows a programmed ramp starting at 60 °C, increasing at 3 °C/min, and reaching up to 240 °C. Finally, the sample encounters the elevated temperatures of the mass spectrometry (MS) detector’s source (250 °C) and interface (280 °C). Even in isocratic methods, where the oven temperature remains constant throughout the analysis, the inlet, source, and interface temperatures are maintained at high levels. Although the sample passes through these stages briefly, the elevated temperatures can induce Cope rearrangements in the essential oil, leading to possible changes in its composition. <a href="javascript:void(0);">(22,23)</a>The accurate characterization of the chemical composition of essential oils is crucial for any study employing them as a biological or analytical matrix, as it supports the interpretation of bioactivity, chemotaxonomic classification, and quality control of samples with economic value added. There are many studies attributing relevant biological activities, classifying specimens, and identifying phenotypic and genetic variations based on the chemical composition of the essential oil of E. uniflora L., which is usually characterized by GC-MS. <a href="javascript:void(0);">(8,9,11,24)</a> As an example of the study carried out by de Jesus, found acute anti-inflammatory effect of a rich in curzerene essential oil. <a href="javascript:void(0);">(5)</a> Similarly, Pascoal, reported distinct essential oil composition patterns among E. uniflora varieties─yellow, red, and purple fruits─primarily driven by variations in β-Elemene and germacrene D content. <a href="javascript:void(0);">(7)</a> These findings highlight metabolic changes during fruit ripening and underscore the influence of genetic diversity among E. uniflora varieties. Such exhibitions are unsatisfactory, because they sustain all their evidence in the characterization of their essential oil only by GC-MS analysis, without considering the Cope rearrangements, a fact that may change the outcome of their research. In this context Nuclear Magnetic Resonance (NMR) spectroscopy is a good alternative for essential oil analysis, since is a robust not destructive technique and able to detect and quantify simultaneously a wide range of metabolites that exceed the concentration of about 5–10 μM. <a href="javascript:void(0);">(25)</a>In order to highlight analytical concerns about the uses of only GC-MS data to access chemical relevance of E. uniflora essential oil studies, Nuclear Magnetic Resonance (NMR) spectroscopy was employed to evaluate the chemical composition of the essential oil of Eugenia uniflora L. before and after an induced thermal treatment, compared to GC-MS data. The findings provide insights into thermolabile compounds and highlight potential misidentifications of the bioactive properties associated with the sesquiterpenes of E. uniflora present in literature.<h4>2. Results and Discussion</h4><h5>2.1. Characterization of the Essential Oil</h5>Approximately 60 compounds, mostly sesquiterpenes (Germacrene B) and oxygenated sesquiterpenes (Germacrone), were visualized in the essential oil, with the 9 compounds having a relative area above 2%, as shown in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c08966#tbl1">Table 1</a>. The identified and most prevalent compounds align with those reported in the literature for E. uniflora. <a href="javascript:void(0);">(4,11,12)</a> It is possible to highlight the significant proportion of Germacrene-type sesquiterpenes compared to Elemene-type, except Curzerene, which was found in high concentration.<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ACS_Omega_2025_10_48_59425_59434_Table_1_Main_Components_Identified_in_the_GC_MS_Analysis_of_the_Essential_Oil_from_Leaves_of_E_uniflora_9d59d96bef.jpg" alt="ACS Omega 2025, 10, 48, 59425–59434: Table 1. Main Components Identified in the GC–MS Analysis of the Essential Oil from Leaves of E. uniflora." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ACS_Omega_2025_10_48_59425_59434_Table_1_Main_Components_Identified_in_the_GC_MS_Analysis_of_the_Essential_Oil_from_Leaves_of_E_uniflora_9d59d96bef.jpg 218w," sizes="100vw" width="1076" height="771">The variation in the composition of the essential oil from E. uniflora leaves was described in literature, <a href="javascript:void(0);">(9)</a> who classified the specimens into three groups: Group I, containing yellow, dark red, and purple fruits, which showed high concentrations of germacrene B, germacrone, and atractylone; Group II, consisting of light red fruit samples, with high concentrations of curzerene, germacrene D, and germacrene A; and Group III, containing orange-red fruits, with a high content of selina-1,3,7(11)-trien-8-one and oxyselina-1,3,7(11)-trien-8-one. According to this classification, this essential oil fits into Group II.Chemical transformations of many components found in the E. uniflora leaves essential oil result from the heating conditions typically applied during GC–MS analysis, which occur through Cope Rearrangement. <a href="javascript:void(0);">(12,19)</a> Cope rearrangement is a stereospecific [3,3]-sigmatropic rearrangement that proceeds via the most stable chairlike transition state of 1,5-cyclodecadiene, from germacrene-type, to give 1,2-divinylcyclohexane, known as Elemene-type. <a href="javascript:void(0);">(14)</a> Some of the Cope rearrangements found in the E. uniflora essential oil are represented in <a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c08966#fig2">Figure 2</a>. <a href="javascript:void(0);">(11,22,23,26)</a><img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ACS_Omega_2025_10_48_59425_59434_Figure_2_Cope_Rearrangements_of_sesquiterpenes_7fe9282d75.jpg" alt="ACS Omega 2025, 10, 48, 59425–59434: Figure 2. Cope Rearrangements of sesquiterpenes." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ACS_Omega_2025_10_48_59425_59434_Figure_2_Cope_Rearrangements_of_sesquiterpenes_7fe9282d75.jpg 150w," sizes="100vw" width="1500" height="1566">The same essential oil was analyzed using NMR spectroscopy to identify its components. Although NMR identification is considerably more labor-intensive than GC-MS analysis, it offers the advantage of being a cold and nondestructive technique. Since the sample does not undergo heating during the process, its stability is preserved throughout the analysis. The conformational differences observed in germacrene-type compounds further increase the spectrum’s complexity, leading to signal broadening in the 1H NMR spectra. <a href="javascript:void(0);">(27)</a>A substantial number of signals were observed in the 1H spectrum, with the majority concentrated between 0.5 and 3.0 ppm, a region characteristic of terpene compounds. The region between 4.5 and 6.0 ppm also exhibited numerous signals attributed to vinylic protons, observed in sesquiterpenes (<a target="_blank" rel="noopener noreferrer" href="https://pubs.acs.org/doi/10.1021/acsomega.5c08966#fig3">Figure 3</a>).<img src="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/ACS_Omega_2025_10_48_59425_59434_Figure_3_1_H_NMR_400_13_M_Hz_CD_Cl3_spectra_of_the_raw_essential_oil_a46e04574e.jpg" alt="ACS Omega 2025, 10, 48, 59425–59434: Figure 3. 1H NMR (400.13 MHz, CDCl3) spectra of the raw essential oil." srcset="https://storage.googleapis.com/labrulez-bucket-strapi-h3hsga3/thumbnail_ACS_Omega_2025_10_48_59425_59434_Figure_3_1_H_NMR_400_13_M_Hz_CD_Cl3_spectra_of_the_raw_essential_oil_a46e04574e.jpg 245w," sizes="100vw" width="4175" height="2376"><h4>3. Conclusions</h4>The investigation of the composition of E. uniflora essential oil by NMR and the thermal treatment performed proved that curzerene may come from furanodiene due to the transformations that occur in the matrix during gas chromatographic analysis. These findings have significant implications for the investigation into the chemical composition of E. uniflora essential oil and the evaluation of the biological properties of its sesquiterpenes. Since each technique has advantages and disadvantages, combining GC-MS analysis with a cold technique, such as NMR is important to guarantee the proper identification of the compound genuinely responsible for any property assigned to E. uniflora essential oil.<h4>4. Materials and Methods</h4><h5>4.2. GC-MS Analysis</h5>The gas chromatographic analyses of the essential oils (10 mg mL–1) were performed using a gas chromatography–mass spectrometry system (<a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/library?mainauthorItems=1&amp;search=QP2020">Shimadzu GCMS-QP2020 Gas Chromatograph</a>). The analyses were conducted on an RTx-5MS capillary column (30 m × 0.25 mm internal diameter × 0.25 μm film thickness), and the analytical conditions were as follows: split ratio of 1/10, injector temperature at 250 °C, ion source at 250 °C, and interface at 280 °C. The temperature program of the oven was set at 60 °C for 5 min, followed by a temperature ramp of 3 °C/min until reaching the final temperature of 240 °C. The components were identified based on the relative retention index, calculated for each constituent by injecting a series of n-alkane standards (C8–C20) under the same sample conditions and comparing them with tabulated values as well as by comparing the obtained mass spectra with the mass spectra database and literature comparisons. <a href="javascript:void(0);">(21)</a><h5>4.4. NMR Analysis</h5>All NMR spectra were acquired at 298 K on a Bruker AVANCE III spectrometer operating at 9.4 T, observing 1H at 400.13 MHz and 13C at 100.13 MHz, equipped with a broadband probe. The essential oil was solubilized in CDCl3 with 0.05% of tetramethylsilane (TMS) used as an internal reference. The 1H NMR spectra were recorded utilizing 65k time-domain data points across a spectral width of 20.00 ppm. This setup provided a digital resolution of 0.24 Hz. The data were obtained using a single 30° excitation pulse, with a relaxation delay of 1.0 s, and an average of 128 scans. The 13C NMR spectra was carried out using the zgpg30 pulse sequence utilizing 64k time-domain data points across a spectral width of 238 ppm, with an acquisition time of 1.3631 s, providing a digital resolution of 0.7434 Hz and a relaxation delay of 2.0s and an average of 2k scans.The HSQC and HMBC experiments were conducted using standard pulse sequences from the Bruker library, with modifications to the number of acquired points to improve resolution, 2048 in F2 and 512 in F1.</div>

Is Curzerene Responsible for the Bioactive Properties of Eugenia uniflora? A Possible Misinterpretation of Bioactive Markers

Quantitative Assessment of Chemical Modifications of Macromolecules through Counterion Measurement

In the week of March 30, 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. Agilent Technologies: Trace the Threat: Py-GC/MS Workflows for Microplastics Characterization</h5><ul><li>Tu, 31.3.2026 06:30 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/6025">Registration</a></li></ul>Discover advanced approaches for trace micro- and nanoplastics analysis using Py-GC/MS and explore how the Agilent 5977C GC/MSD enhances sensitivity, robustness, and workflow efficiency.<h5>2. Thermo Fisher Scientific: FTIR microscopy: Practical guidance for effective sample analysis</h5><ul><li>Tu, 31.3.2026 17:00 CEST</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/6088">Registration</a></li></ul>Join this webinar to gain practical guidance on FTIR microscopy workflows, including measurement modes, sample preparation, parameter optimization and spectral interpretation.<h5>3. Bruker: Understanding Polymer Reactions and Degradation with FT-IR and EPR Spectroscopy</h5><ul><li>Tu, 31.3.2026 17:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5996">Registration</a></li></ul>Discover how FT-IR and EPR spectroscopy reveal polymer curing kinetics and radical-driven mechanisms—enabling real-time monitoring, degree of cure quantification, and stability studies.<h5>4. Technology Networks: Advances in Hydrogen Gas Generation for Sustainable Laboratories</h5><ul><li>Tu, 31.3.2026 17:00 CET</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/5941">Registration</a></li></ul>Discover how modern hydrogen gas generators support high-purity GC performance while reducing costs and environmental impact. Learn how on-site generation improves uptime, efficiency, and lab sustainability.<h5>5. C&amp;EN: Overcoming Raman Microscopy Challenges in Microplastics and Life Sciences</h5><ul><li>We, 1.4.2026 17:00 CEST</li><li><a target="_blank" rel="noopener noreferrer" href="https://gcms.labrulez.com/webinar/6016">Registration</a></li></ul>Learn how O-PTIR spectroscopy overcomes fluorescence limitations in Raman microscopy. Discover simultaneous sub-micron IR and Raman analysis for microplastics, biological samples, and organic materials.</div></div></div></div></div></div>

Webinars LabRulezGCMS Week 14/2026

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Agilent Technologies

GERSTEL

Wiley

Thousands of polymeric compounds and materials have been developed over the years to optimize the properties and performance of products spanning nearly every industry. There are a few areas where characterizing these products can be important: first is performing a quick polymer identification for recycling purposes; second is quality control to identify product defects or failures; and third is reverse engineering to facilitate product development in a highly competitive marketplace.
Infrared (IR) and Raman spectroscopy are especially useful for the analysis of polymers in an industrial setting because in most cases it does not require sample preparation or expensive consumables. Examples will be presented demonstrating the effectiveness of IR and Raman analysis in each of these categories.
Mass Spectrometry (MS) has become an indispensable tool for polymer analysis and has been widely used to study polymer structure and composition, end groups and additives, molecular weight distribution, and so on. MS analysis is extremely sensitive, allowing the detection and identification of minor polymer components and synthesis by-products, as well as low-level impurities and products of decomposition. Matrix Assisted Laser Desorption Ionization (MALDI) allows performing rapid MS analysis without lengthy pre-separation and with minimal sample preparation. MALDI MS can provide structural and copolymer composition information, as well as be used for imaging of polymer surfaces, characterization of complex polymer mixtures, and many other analytical tasks.
In this webinar, we will discuss several MS analytical techniques and their applications for polymer analysis using real-life examples from the industry and academia.
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Presenter: Sergey V. Shilov, Ph.D. (R&amp;D Product Manager for North America, Bruker Optics)
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Dr. Sergey V. Shilov is the R&amp;D Product Manager for North America at Bruker Optics. Sergey joined Bruker in 2001. He is responsible for the support and development of new applications for the Bruker research FTIR systems. He received his Ph.D in 1992 from the Russian Academy of Sciences in Polymer Physics and his M.S. from St. Petersburg State University (Russia) in Physics in 1986. Alexander Von Humboldt foundation (Germany) awarded him research fellowship in 1996. Sergey published 37 papers in peer-reviewed journals. His research interests include time-resolved FTIR spectroscopy, surface science, polymer and life-science applications. 
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Presenter: Kushal Modi (Business Development Manager, Polymers, and Industrial Chemicals, Bruker Applied Mass Spectrometry)
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Kushal Modi has been serving the scientific community for over 10 years. He joined Bruker in 2022 under the Applied Mass Spectrometry division after a legacy with Waters Corporation. He is a leading expert as a Business Development Manager and is currently supporting the polymers and industrial chemical markets nationally. 
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Presenter: Dr. Rebecca Pool (Editor Microscopy and Analysis, Wiley, Moderator)
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Rebecca is news editor of Microscopy&amp;Analysis and a freelance science journalist with a doctorate in Materials Science. She has published in Wiley Analytical Science, Nature Photonics, SPIE Photonics Focus, Physics World, Sci Fi Generation, Engineering and Technology magazine, WorldSteel and more.
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Wiley Analytical Science: Effective Analysis of Polymers Using IR, Raman Spectroscopy, and MALDI-TOF Mass Spectrometry

Effective Analysis of Polymers Using IR, Raman Spectroscopy, and MALDI-TOF Mass Spectrometry

Examples will be presented demonstrating the effectiveness of IR and Raman analysis and will discuss several MS techniques and apps for polymer analysis.

Polymers Using IR, Raman Spectroscopy, and MALDI-TOF MS

The easy-to-use 8700 LDIR has undergone a performance enhancements with the addition of automated on-filter analysis. This improvement will be described in this webinar and the results of analyses will be presented.
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Presenter: Louis Tisinger, PhD (Application Engineer, Molecular Spectroscopy, Agilent Technologies, Inc.)
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Louis (Lou) Tisinger has a Ph.D. in Analytical Chemistry from Miami University in Oxford Ohio, where his graduate research involved the study of ATR imaging and microscope performance in vibrational spectroscopy. Most of his career has been related to pre- and post-sales support of FTIR spectrometers, microscopes, imaging systems, and thermal analytical instruments, focusing on analyzing customer samples, demonstrations, post-sales training, troubleshooting, and R&amp;D.
</blockquote>

Agilent Technologies: New LDIR Enhancements to Streamline Microplastics Analysis

New LDIR Enhancements to Streamline Microplastics Analysis

The easy-to-use 8700 LDIR has undergone a performance enhancements with the addition of automated on-filter analysis.

Learn how to automate your SPE procedures with the LCTech FREESTYLE™ system for various sample types.
Presenter: Fred Foster (Applications Scientist)

GERSTEL: Automation of Solid Phase Extraction Procedures using a Novel Robotic Automation Platform

Automation of Solid Phase Extraction Procedures using a Novel Robotic Automation Platform

Learn how to automate your SPE procedures with the LCTech FREESTYLE™ system for various sample types.

Automation of Solid Phase Extraction - Automation Platform

This Seminar is designed to help chemists and lab managers become more familiar with the workings of Agilent’s newest software - OpenLab CDS.
Participants will listen to an Agilent expert and watch a series of live demonstrations.They will have amble opportunity to ask their own specific questions during the course of this seminar. Customers that are new to OpenLab CDS or are using an older software package from Agilent such as ChemStation would benefit from seeing the future of their laboratory software.
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Presenter: Richard Mutkoski (Laboratory Informatics Application Engineer, Agilent Technologies, Inc.)
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Richard Mutkoski began with Agilent (HP) in 1995. He has been an Application Engineer in Agilent’s Laboratory Informatics for the past 18 years. Prior to his career at Agilent Rich spent 12 years in a variety of small pharmaceutical firms in both R&amp;D and QA/QC capacities affording him first-hand knowledge of those workflows, bottlenecks and challenges.
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Agilent Technologies: Get The Most Out of Your OpenLab CDS System – An Exploration of Agilent’s Newest Chromatography Data System

Get The Most Out of Your OpenLab CDS System – An Exploration of Agilent’s Newest Chromatography Data System

Become more familiar with the workings of Agilent’s newest software - OpenLab CDS.

Get The Most Out of Your OpenLab CDS System

Learn about the function and advantages of the new control panel including creating instruments, creating projects, activity logs, storage types and paths.
Learn the basic operations of user privileges including assigning permissions and roles, and license utilities.
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Presenter: Richard Mutkoski (Laboratory Informatics Application Engineer, Agilent Technologies, Inc.)
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Richard Mutkoski has been a field representative for over 27 years for both hardware and software. In his current role as an Informatics Application Engineer, Rich presents technical solutions of the OpenLab suite of products to customers worldwide. Prior to his tenure at Agilent Rich spent 15 years in a variety of Pharma QA/QC and R&amp;D positions providing him a unique understanding of those workflows, bottlenecks and challenges.
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Agilent Technologies: Openlab CDS ChemStation Edition - Getting Started

Openlab CDS ChemStation Edition - Getting Started

Learn about the function and advantages of the new control panel including creating instruments, creating projects, activity logs, storage types and paths.

The FDA guidance for Computer System Assurance (CSA) is intended to reduce the time and effort of the Computerized System Validation (CSV) process without compromising regulatory compliance or data integrity.
The regulated life science industries generally consider the CSV process as burdensome and as a hindrance to adopting new automation technologies that could greatly improve the efficiency and productivity of their business. In this presentation we will examine the six major points of the CSA guidance and how they can be used to improve your CSV process. We will also examine Agilent’s validation services, our process efficiencies, and how we intend to integrate elements of the CSA guidance.
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Presenter: Michael Korbel (Sr. Compliance Consultant, Agilent Technologies, Inc.)
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Michael has over 22 years of experience in regulated environments in the pharmaceutical and bio-tech industries. Half of Michael&#39;s career has been spent on the customer side of the industry in both IT and laboratory positions, supporting, qualifying, and validating regulated instruments and computerized systems. The other half has been spent providing consultative compliance service programs from the vendor side of the industry. His experience includes technical support and validation of both standalone and enterprise laboratory informatics systems, as well as instrument qualification, preventive maintenance, and relocation services. Michael’s current role at Agilent Technologies is to create new compliance consulting services for our regulated customers and implement them globally. Michael holds a B.S. in Biology, with minors in Chemistry and Environmental Science.
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Agilent Technologies: New FDA guidance “Computer System Assurance” and Agilent Validation Service Offerings

New FDA guidance “Computer System Assurance” and Agilent Validation Service Offerings

The six major points of the CSA guidance and how they can be used to improve your CSV process.

New FDA guidance “Computer System Assurance”

Now that you are using the OpenLab CDS system, why are you still using Excel?
Unlock the incredible calculation potential of your system. You have run a triplicate injection of standards and would like to determine the percent recovery of your samples against the average of those standards. This session will introduce you to the method of being able to do just that within OpenLab CDS WITHOUT the use of Excel.
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Presenter: Richard Mutkoski (Laboratory Informatics Application Engineer, Agilent Technologies, Inc.)
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Richard Mutkoski has been a field representative for over 27 years for both hardware and software. In his current role as an Informatics Application Engineer, Rich presents technical solutions of the OpenLab suite of products to customers worldwide. Prior to his tenure at Agilent Rich spent 15 years in a variety of Pharma QA/QC and R&amp;D positions providing him a unique understanding of those workflows, bottlenecks and challenges.
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Agilent Technologies: Calculate Percent Recovery of Samples in OpenLab CDS

Calculate Percent Recovery of Samples in OpenLab CDS

The method of being able to do just that within OpenLab CDS WITHOUT the use of Excel.

This seminar introduces a powerful feature in OpenLab CDS: Custom Calculator.
OpenLab CDS users or chromatographers thinking of moving to OpenLab CDS from another data system can see how this unique feature allows the addition of user defined chromatography calculations directly into the OpenLab CDS data system.
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Presenter: Kathleen O&#39;Dea (Application Engineer, Agilent Technologies, Inc.)
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Kathleen O’Dea has a 20 year history with Agilent’s OpenLab products. As an Informatics Application Engineer, Kathleen has visited customers around the world in a wide variety of market areas, helping them to select and implement OpenLab software products.
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Agilent Technologies: Introducing the Custom Calculator in OpenLab CDS

Introducing the Custom Calculator in OpenLab CDS

Powerful feature in OpenLab CDS: Custom Calculator.

Are you an analyst, manager, or reviewer who needs to get work done but may not be in the lab?
Especially important today, remote access is a key feature that can increase productivity, reduce compliance costs and is a key part of a disaster recovery plan. This virtual seminar introduces options for thin client technology enabling all Masshunter, ChemStation or OpenLab CDS products to be accessed outside the lab, whether this is at from nearby desks, across sites, or from home.
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Presenter: Mike Ratto (Lab Informatics Applications Specialist, Agilent Technologies, Inc.)
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Mike Ratto has been with Agilent for 29 years as a field representative for both hardware and software products. In his current role as an Informatics Application Specialist, Mike presents technical solutions of OpenLab family of products to customers all over the world.
</blockquote>

Agilent Technologies: Agilent Software products and Architecture to enable work from home options

Agilent Software products and Architecture to enable work from home options

Options for thin client technology enabling all Masshunter, ChemStation or OpenLab CDS products to be accessed outside the lab.

Agilent Software products and Architecture to enable work

Are you an analyst, manager, or reviewer who follows the social distancing guidelines but need to get work done without full access to your lab?
Especially important today, Remote Access is a key feature that can increase productivity, reduce compliance costs and can be an integral part of a disaster recovery plan. This virtual seminar introduces options using “Thin Client technology which enables all Masshunter, ChemStation or OpenLab CDS products to be accessed outside the lab, whether this is at from nearby desks, across sites, or from home.
Our learning objectives during this 1 hour session are as follows:
<ul>
<li>An introduction to “Thin Client” technology
</li>
<li>Data and instrument access options from lab, office or home with OpenLab
</li>
<li>Learn technology options that support Social Distancing in the laboratory
</li>
</ul>
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Presenter: Mike Ratto (Lab Informatics Applications Specialist, Agilent Technologies, Inc.)
</blockquote>
<blockquote>
Mike Ratto has been with Agilent for 29 years as a field representative for both hardware and software products. In his current role as an Informatics Application Specialist, Mike presents technical solutions of OpenLab family of products to customers all over the world.
</blockquote>

Agilent Technologies: OpenLab CDS/ECM Remote Access Solutions to support Social Distancing in the Lab

OpenLab CDS/ECM Remote Access Solutions to support Social Distancing in the Lab

Options using “Thin Client technology which enables all Masshunter, ChemStation or OpenLab CDS products to be accessed outside the lab.