View Future GrowthThis company listing is no longer activeThis company may still be operating, however this listing is no longer active. Find out why through their latest events.See Latest EventsRevvity 과거 순이익 실적과거 기준 점검 0/6Revvity의 수입은 연평균 -31.7%의 비율로 감소해 온 반면, Life Sciences 산업은 수입이 연평균 3.2% 증가했습니다. 매출은 연평균 8%의 비율로 감소해 왔습니다. Revvity의 자기자본이익률은 3.2%이고 순이익률은 8.3%입니다.핵심 정보-31.70%순이익 성장률-33.81%주당순이익(EPS) 성장률Life Sciences 산업 성장률26.83%매출 성장률-7.98%자기자본이익률3.15%순이익률8.26%최근 순이익 업데이트28 Sep 2025최근 과거 실적 업데이트Reported Earnings • Oct 28Third quarter 2025 earnings released: EPS: US$0.41 (vs US$0.76 in 3Q 2024)Third quarter 2025 results: EPS: US$0.41 (down from US$0.76 in 3Q 2024). Revenue: US$698.9m (up 2.2% from 3Q 2024). Net income: US$47.2m (down 49% from 3Q 2024). Profit margin: 6.8% (down from 14% in 3Q 2024). Revenue is forecast to grow 5.1% p.a. on average during the next 3 years, compared to a 9.6% growth forecast for the Life Sciences industry in Europe.공고 • Oct 06Revvity, Inc. to Report Q3, 2025 Results on Oct 27, 2025Revvity, Inc. announced that they will report Q3, 2025 results Pre-Market on Oct 27, 2025공고 • Jul 07Revvity, Inc. to Report Q2, 2025 Results on Jul 28, 2025Revvity, Inc. announced that they will report Q2, 2025 results Pre-Market on Jul 28, 2025모든 업데이트 보기Recent updates공고 • Nov 10Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc.Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc. on November 10, 2025. The transaction is expected to close late in Q4 2025.Reported Earnings • Oct 28Third quarter 2025 earnings released: EPS: US$0.41 (vs US$0.76 in 3Q 2024)Third quarter 2025 results: EPS: US$0.41 (down from US$0.76 in 3Q 2024). Revenue: US$698.9m (up 2.2% from 3Q 2024). Net income: US$47.2m (down 49% from 3Q 2024). Profit margin: 6.8% (down from 14% in 3Q 2024). Revenue is forecast to grow 5.1% p.a. on average during the next 3 years, compared to a 9.6% growth forecast for the Life Sciences industry in Europe.공고 • Oct 27+ 1 more updateRevvity, Inc. (NYSE:RVTY) announces an Equity Buyback for $1,000 million worth of its shares.Revvity, Inc. (NYSE:RVTY) announces a share repurchase program. Under the program, the company will repurchase up to $1,000 million worth of its own shares. The program is valid for 2 years.공고 • Oct 25Revvity, Inc. Appoints Anita Gonzales as Vice President and Chief Accounting Officer, Effective October 23, 2025On October 23, 2025, the Board of Directors of Revvity, Inc. appointed Anita Gonzales, the Company’s Vice President and Controller, to serve as its Vice President and Chief Accounting Officer, effective October 23, 2025. Mrs. Gonzales, 49, has served as the Company’s Vice President and Controller since May 2023, having joined the Company as Senior Director of Integration and Controllership Initiatives in March 2021. Prior to joining the Company, Mrs. Gonzales was at General Electric Company (“GE”) for ten years. During her tenure at GE, Mrs. Gonzales was Director of Audit and Advisory Practices Corporate division from 2016 to 2021, with responsibility for technical accounting and audit standards of the Corporate Audit Staff. Before that, Mrs. Gonzales held executive roles at GE Aviation including Global Controller-Commercial Engines. Earlier in her career, she held roles of increasing responsibility, up to Senior Manager, at PricewaterhouseCoopers. Mrs. Gonzales holds Master of Public Accounting and Bachelor of Business Administration degrees from the University of Texas at Austin and is a Certified Public Accountant.공고 • Oct 24Revvity Board Declares Quarterly Dividend, Payable on February 6, 2026The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on February 6, 2026 to all shareholders of record at the close of business on January 16, 2026.공고 • Oct 06Revvity, Inc. to Report Q3, 2025 Results on Oct 27, 2025Revvity, Inc. announced that they will report Q3, 2025 results Pre-Market on Oct 27, 2025공고 • Sep 30Revvity, Inc. Unveils New AI Software Offering to Transform Preclinical Imaging AnalysisRevvity, Inc. announced the launch of its Living Image Synergy AI multimodal analysis software for in vivo imaging researchers. The solution provides a unified platform with AI capabilities for seamless data analysis across optical, microCT, ultrasound, and other modalities--reducing data inconsistencies, streamlining workflows, increasing throughput, and enhancing reproducibility, all with the intention of accelerating scientific discovery. The Living Image Synergy AI software centralizes analysis with a goal of eliminating the need for separate tools and enabling seamless correlation of datasets. Revvity developed this unified approach to help researchers uncover biological insights that might otherwise remain hidden when using isolated systems. To further streamline workflows, the software features intuitive co-registration tools and automated processes that reduce manual tasks and analysis time. Advanced AI algorithms automate image segmentation and region-of-interest (ROI) quantification--traditionally labor-intensive and variable steps in imaging analysis. This helps support high-throughput analysis and allows researchers to more efficiently monitor disease progression and assess therapeutic efficacy with greater accuracy and statistical confidence.공고 • Sep 22Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)공고 • Aug 07Revvity Launches Innovative Reagent Technology to Accelerate Development of Next-Generation Targeted TherapeuticsRevvity, Inc. announced the launch of pHSense™? reagents, a powerful technology designed to advance internalization studies in drug discovery. pHSense reagents are designed for high-throughput, plate-based workflows and intended for researchers studying G protein-coupled receptors (GPCRs) or antibody-drug conjugates (ADCs). They offer a scalable, accurate, and easy-to-implement solution for monitoring antibody, ADC, or receptor internalization. Developed for use with standard plate readers, pHSense reagents combine a pH-sensitive dye and a time-resolved fluorescence (TRF) readout to allow for the delivery of robust kinetics of internalization and high signal-to- background--even at low endogenous receptor expression levels. Fully compatible with Revvity's multimode detection platforms, pHSense reagents have the potential to significantly enhance detection capability while simplifying integration into existing drug discovery workflows. By enabling more efficient screening and characterization of promising therapeutic candidates, pHSense reagents can help researchers accelerate preclinical development timelines, potentially reducing overall development costs and contributing to more efficient advancement of candidates toward clinical evaluation. With a growing focus on receptor trafficking in drug development and increasing demand for accurate, high-throughput tools, pHSense reagents offer support for emerging trends in oncology and precision medicine, particularly in ADC development. The innovative design focused on addressing major limitations of current offerings such as low throughput and suboptimal signal-to-noise ratios.공고 • Jul 29Revvity, Inc. Updates Earnings Guidance for the Full Year Ending December 28, 2025Revvity, Inc. updated earnings guidance for the full year ending December 28, 2025. The company is raising its revenue guidance to a range of $2.84 billion to $2.88 billion to reflect recent changes in foreign currency exchange rates and assumes 2% to 4% organic growth.공고 • Jul 25Revvity, Inc. Declares Quarterly Dividend, Payable on November 7, 2025The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on November 7, 2025 to all shareholders of record at the close of business on October 17, 2025.공고 • Jul 07Revvity, Inc. to Report Q2, 2025 Results on Jul 28, 2025Revvity, Inc. announced that they will report Q2, 2025 results Pre-Market on Jul 28, 2025공고 • Jun 02Revvity, Inc. Introduces New IVD Reference Standards for Monitoring Oncology Diagnostic Testing WorkflowsRevvity, Inc. announced the launch of three Mimix reference standards for IVD use, designed for monitoring of next-generation sequencing (NGS) or droplet digital polymerase chain reacting (ddPCR) assays designed to detect somatic mutations in genomic DNA (gDNA) from human samples for IVD use. These cell line-derived reference standards have undergone appropriate design controls to meet U.S. Food and Drug Administration (FDA) regulatory requirements, which helps laboratories integrate them into existing workflows to support monitoring test performance, assay variation, and to help identify increases in random or systemic errors. Offering the Mimix reference standards for IV D indicates the products have been developed and manufactured in accordance with applicable quality system requirements allowing for improved reliability and precision of these reference standards. The three Mimix reference standards cover key cancer testing applications, which include: Mimix OncoSpan FFPE Reference Standard IVD (HD832-IVD); Mimix OncoSpan gDNA Reference Standard IVD (HD 827-IVD); Mimix Myeloid Cancer Panel, gDNA Reference Standard IVD.공고 • May 20Revvity's EUROIMMUN Unveils New Fully Automated Instrument for Specialty TestingRevvity, Inc. announced the launch of its new IDS i20™? analytical random access platform from EUROIMMUN, enabling full automation of chemiluminescence immunoassays (ChLIA). The IDS i20 platform is a CE marked and FDA listed device that allows laboratories to consolidate multiple specialty tests on a unique single instrument with greater reagent capacity and higher test throughput compared to existing offerings. The highly versatile IDS i20 instrument allows users to simultaneously run 20 analytes from six diagnostic specialties on a single device. These specialties include endocrinology, allergy, autoimmune and infectious disease testing, testing for Alzheimer's disease and therapeutic drug monitoring. While specialty assays in these diagnostic areas tend to be processed manually or with semi-automated, low-throughput analyzers, the IDS i20 platform offers labs a new means of more flexible, fully automated ChLIA processing. With the ability to process up to 140 tests per hour (assay dependent), the IDS i20 instrument is the latest addition to the well-established IDS i-device series, built on more than 50 years of experience in medical device design and innovation. The IDS i20 platform features new software offering a high degree of adaptability and scalability, along with a superior graphical user interface that meets the latest standards of ergonomics, usability and cybersecurity. Continuous loading of samples and reagents as well as the integrated cooling of ready-to-use reagent cartridges allow for non-stop operation of the system - maximizing efficiency and minimizing hands-on time.매출 및 비용 세부 내역Revvity가 돈을 벌고 사용하는 방법. 최근 발표된 LTM 실적 기준.순이익 및 매출 추이BIT:1RVTY 매출, 비용 및 순이익 (USD Millions)날짜매출순이익일반관리비연구개발비28 Sep 252,81323292820929 Jun 252,79827993620730 Mar 252,77029693920129 Dec 242,75528393119729 Sep 242,72225894919930 Jun 242,70819794220231 Mar 242,72618394321131 Dec 232,75118094221701 Oct 232,79621389822202 Jul 232,83725090322202 Apr 233,02435391822101 Jan 233,31251394022202 Oct 223,5995991,00122203 Jul 223,74863798921903 Apr 223,48369488519502 Jan 223,82888985420003 Oct 214,1551,08689319704 Jul 214,2571,15589319704 Apr 214,4381,07496121703 Jan 212,66363172914604 Oct 203,23441288719605 Jul 202,97729486619105 Apr 202,88722684519029 Dec 192,88422883318929 Sep 192,83523580619430 Jun 192,80225179419731 Mar 192,78324779019630 Dec 182,77823780919430 Sep 182,66312876118001 Jul 182,54314971916601 Apr 182,38714766715231 Dec 172,25715761513901 Oct 172,18225858713502 Jul 172,14221558012902 Apr 172,13221058412801 Jan 172,11621658512402 Oct 161,99919857410803 Jul 162,04819958311003 Apr 162,07619058311003 Jan 162,10518958611304 Oct 152,26317666112728 Jun 152,24116465712629 Mar 152,23416765612428 Dec 142,070130648108양질의 수익: 1RVTY는 $75.9M 규모의 큰 일회성 손실이 있어 28th September, 2025까지 지난 12개월 재무 결과에 영향을 미쳤습니다.이익 마진 증가: 1RVTY의 현재 순 이익률 (8.3%)은 지난해 (9.5%)보다 낮습니다.잉여현금흐름 대비 순이익 분석과거 순이익 성장 분석수익추이: 1RVTY의 수익은 지난 5년 동안 연평균 31.7% 감소했습니다.성장 가속화: 1RVTY은 지난 1년 동안 수익이 감소하여 5년 평균과 비교할 수 없습니다.수익 대 산업: 1RVTY은 지난 1년 동안 수익이 감소(-9.7%)하여 Life Sciences 업계 평균(13.3%)과 비교하기 어렵습니다.자기자본이익률높은 ROE: 1RVTY의 자본 수익률(3.2%)은 낮음으로 평가됩니다.총자산이익률투하자본수익률우수한 과거 실적 기업을 찾아보세요7D1Y7D1Y7D1YPharmaceuticals-biotech 산업에서 과거 실적이 우수한 기업.View Financial Health기업 분석 및 재무 데이터 상태데이터최종 업데이트 (UTC 시간)기업 분석2025/11/26 18:17종가2025/11/21 00:00수익2025/09/28연간 수익2024/12/29데이터 소스당사의 기업 분석에 사용되는 데이터는 S&P Global Market Intelligence LLC에서 제공됩니다. 아래 데이터는 이 보고서를 생성하기 위해 분석 모델에서 사용됩니다. 데이터는 정규화되므로 소스가 제공된 후 지연이 발생할 수 있습니다.패키지데이터기간미국 소스 예시 *기업 재무제표10년손익계산서현금흐름표대차대조표SEC 양식 10-KSEC 양식 10-Q분석가 컨센서스 추정치+3년재무 예측분석가 목표주가분석가 리서치 보고서Blue Matrix시장 가격30년주가배당, 분할 및 기타 조치ICE 시장 데이터SEC 양식 S-1지분 구조10년주요 주주내부자 거래SEC 양식 4SEC 양식 13D경영진10년리더십 팀이사회SEC 양식 10-KSEC 양식 DEF 14A주요 개발10년회사 공시SEC 양식 8-K* 미국 증권에 대한 예시이며, 비(非)미국 증권에는 해당 국가의 규제 서식 및 자료원을 사용합니다.별도로 명시되지 않는 한 모든 재무 데이터는 연간 기간을 기준으로 하지만 분기별로 업데이트됩니다. 이를 TTM(최근 12개월) 또는 LTM(지난 12개월) 데이터라고 합니다. 자세히 알아보기.분석 모델 및 스노우플레이크이 보고서를 생성하는 데 사용된 분석 모델의 세부 정보는 당사의 GitHub 페이지에서 확인하실 수 있습니다. 또한 보고서 사용 방법에 대한 가이드와 YouTube 튜토리얼도 제공하고 있습니다.Simply Wall St 분석 모델을 설계하고 구축한 세계적 수준의 팀에 대해 알아보세요.산업 및 섹터 지표산업 및 섹터 지표는 Simply Wall St가 6시간마다 계산하며, 프로세스에 대한 자세한 내용은 Github에서 확인할 수 있습니다.분석가 소스Revvity, Inc.는 34명의 분석가가 다루고 있습니다. 이 중 16명의 분석가가 우리 보고서에 입력 데이터로 사용되는 매출 또는 수익 추정치를 제출했습니다. 분석가의 제출 자료는 하루 종일 업데이트됩니다.분석가기관Catherine Ramsey SchulteBairdCharles ButlerBarclaysLuke SergottBarclays31명의 분석가 더 보기
Reported Earnings • Oct 28Third quarter 2025 earnings released: EPS: US$0.41 (vs US$0.76 in 3Q 2024)Third quarter 2025 results: EPS: US$0.41 (down from US$0.76 in 3Q 2024). Revenue: US$698.9m (up 2.2% from 3Q 2024). Net income: US$47.2m (down 49% from 3Q 2024). Profit margin: 6.8% (down from 14% in 3Q 2024). Revenue is forecast to grow 5.1% p.a. on average during the next 3 years, compared to a 9.6% growth forecast for the Life Sciences industry in Europe.
공고 • Oct 06Revvity, Inc. to Report Q3, 2025 Results on Oct 27, 2025Revvity, Inc. announced that they will report Q3, 2025 results Pre-Market on Oct 27, 2025
공고 • Jul 07Revvity, Inc. to Report Q2, 2025 Results on Jul 28, 2025Revvity, Inc. announced that they will report Q2, 2025 results Pre-Market on Jul 28, 2025
공고 • Nov 10Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc.Revvity, Inc. (NYSE:RVTY) entered into a definitive agreement to acquire Advanced Chemistry Development, Inc. on November 10, 2025. The transaction is expected to close late in Q4 2025.
Reported Earnings • Oct 28Third quarter 2025 earnings released: EPS: US$0.41 (vs US$0.76 in 3Q 2024)Third quarter 2025 results: EPS: US$0.41 (down from US$0.76 in 3Q 2024). Revenue: US$698.9m (up 2.2% from 3Q 2024). Net income: US$47.2m (down 49% from 3Q 2024). Profit margin: 6.8% (down from 14% in 3Q 2024). Revenue is forecast to grow 5.1% p.a. on average during the next 3 years, compared to a 9.6% growth forecast for the Life Sciences industry in Europe.
공고 • Oct 27+ 1 more updateRevvity, Inc. (NYSE:RVTY) announces an Equity Buyback for $1,000 million worth of its shares.Revvity, Inc. (NYSE:RVTY) announces a share repurchase program. Under the program, the company will repurchase up to $1,000 million worth of its own shares. The program is valid for 2 years.
공고 • Oct 25Revvity, Inc. Appoints Anita Gonzales as Vice President and Chief Accounting Officer, Effective October 23, 2025On October 23, 2025, the Board of Directors of Revvity, Inc. appointed Anita Gonzales, the Company’s Vice President and Controller, to serve as its Vice President and Chief Accounting Officer, effective October 23, 2025. Mrs. Gonzales, 49, has served as the Company’s Vice President and Controller since May 2023, having joined the Company as Senior Director of Integration and Controllership Initiatives in March 2021. Prior to joining the Company, Mrs. Gonzales was at General Electric Company (“GE”) for ten years. During her tenure at GE, Mrs. Gonzales was Director of Audit and Advisory Practices Corporate division from 2016 to 2021, with responsibility for technical accounting and audit standards of the Corporate Audit Staff. Before that, Mrs. Gonzales held executive roles at GE Aviation including Global Controller-Commercial Engines. Earlier in her career, she held roles of increasing responsibility, up to Senior Manager, at PricewaterhouseCoopers. Mrs. Gonzales holds Master of Public Accounting and Bachelor of Business Administration degrees from the University of Texas at Austin and is a Certified Public Accountant.
공고 • Oct 24Revvity Board Declares Quarterly Dividend, Payable on February 6, 2026The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on February 6, 2026 to all shareholders of record at the close of business on January 16, 2026.
공고 • Oct 06Revvity, Inc. to Report Q3, 2025 Results on Oct 27, 2025Revvity, Inc. announced that they will report Q3, 2025 results Pre-Market on Oct 27, 2025
공고 • Sep 30Revvity, Inc. Unveils New AI Software Offering to Transform Preclinical Imaging AnalysisRevvity, Inc. announced the launch of its Living Image Synergy AI multimodal analysis software for in vivo imaging researchers. The solution provides a unified platform with AI capabilities for seamless data analysis across optical, microCT, ultrasound, and other modalities--reducing data inconsistencies, streamlining workflows, increasing throughput, and enhancing reproducibility, all with the intention of accelerating scientific discovery. The Living Image Synergy AI software centralizes analysis with a goal of eliminating the need for separate tools and enabling seamless correlation of datasets. Revvity developed this unified approach to help researchers uncover biological insights that might otherwise remain hidden when using isolated systems. To further streamline workflows, the software features intuitive co-registration tools and automated processes that reduce manual tasks and analysis time. Advanced AI algorithms automate image segmentation and region-of-interest (ROI) quantification--traditionally labor-intensive and variable steps in imaging analysis. This helps support high-throughput analysis and allows researchers to more efficiently monitor disease progression and assess therapeutic efficacy with greater accuracy and statistical confidence.
공고 • Sep 22Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)Revvity, Inc.(NYSE:RVTY) dropped from FTSE All-World Index (USD)
공고 • Aug 07Revvity Launches Innovative Reagent Technology to Accelerate Development of Next-Generation Targeted TherapeuticsRevvity, Inc. announced the launch of pHSense™? reagents, a powerful technology designed to advance internalization studies in drug discovery. pHSense reagents are designed for high-throughput, plate-based workflows and intended for researchers studying G protein-coupled receptors (GPCRs) or antibody-drug conjugates (ADCs). They offer a scalable, accurate, and easy-to-implement solution for monitoring antibody, ADC, or receptor internalization. Developed for use with standard plate readers, pHSense reagents combine a pH-sensitive dye and a time-resolved fluorescence (TRF) readout to allow for the delivery of robust kinetics of internalization and high signal-to- background--even at low endogenous receptor expression levels. Fully compatible with Revvity's multimode detection platforms, pHSense reagents have the potential to significantly enhance detection capability while simplifying integration into existing drug discovery workflows. By enabling more efficient screening and characterization of promising therapeutic candidates, pHSense reagents can help researchers accelerate preclinical development timelines, potentially reducing overall development costs and contributing to more efficient advancement of candidates toward clinical evaluation. With a growing focus on receptor trafficking in drug development and increasing demand for accurate, high-throughput tools, pHSense reagents offer support for emerging trends in oncology and precision medicine, particularly in ADC development. The innovative design focused on addressing major limitations of current offerings such as low throughput and suboptimal signal-to-noise ratios.
공고 • Jul 29Revvity, Inc. Updates Earnings Guidance for the Full Year Ending December 28, 2025Revvity, Inc. updated earnings guidance for the full year ending December 28, 2025. The company is raising its revenue guidance to a range of $2.84 billion to $2.88 billion to reflect recent changes in foreign currency exchange rates and assumes 2% to 4% organic growth.
공고 • Jul 25Revvity, Inc. Declares Quarterly Dividend, Payable on November 7, 2025The Board of Directors of Revvity, Inc. declared a regular quarterly dividend of $0.07 per share of common stock. This dividend is payable on November 7, 2025 to all shareholders of record at the close of business on October 17, 2025.
공고 • Jul 07Revvity, Inc. to Report Q2, 2025 Results on Jul 28, 2025Revvity, Inc. announced that they will report Q2, 2025 results Pre-Market on Jul 28, 2025
공고 • Jun 02Revvity, Inc. Introduces New IVD Reference Standards for Monitoring Oncology Diagnostic Testing WorkflowsRevvity, Inc. announced the launch of three Mimix reference standards for IVD use, designed for monitoring of next-generation sequencing (NGS) or droplet digital polymerase chain reacting (ddPCR) assays designed to detect somatic mutations in genomic DNA (gDNA) from human samples for IVD use. These cell line-derived reference standards have undergone appropriate design controls to meet U.S. Food and Drug Administration (FDA) regulatory requirements, which helps laboratories integrate them into existing workflows to support monitoring test performance, assay variation, and to help identify increases in random or systemic errors. Offering the Mimix reference standards for IV D indicates the products have been developed and manufactured in accordance with applicable quality system requirements allowing for improved reliability and precision of these reference standards. The three Mimix reference standards cover key cancer testing applications, which include: Mimix OncoSpan FFPE Reference Standard IVD (HD832-IVD); Mimix OncoSpan gDNA Reference Standard IVD (HD 827-IVD); Mimix Myeloid Cancer Panel, gDNA Reference Standard IVD.
공고 • May 20Revvity's EUROIMMUN Unveils New Fully Automated Instrument for Specialty TestingRevvity, Inc. announced the launch of its new IDS i20™? analytical random access platform from EUROIMMUN, enabling full automation of chemiluminescence immunoassays (ChLIA). The IDS i20 platform is a CE marked and FDA listed device that allows laboratories to consolidate multiple specialty tests on a unique single instrument with greater reagent capacity and higher test throughput compared to existing offerings. The highly versatile IDS i20 instrument allows users to simultaneously run 20 analytes from six diagnostic specialties on a single device. These specialties include endocrinology, allergy, autoimmune and infectious disease testing, testing for Alzheimer's disease and therapeutic drug monitoring. While specialty assays in these diagnostic areas tend to be processed manually or with semi-automated, low-throughput analyzers, the IDS i20 platform offers labs a new means of more flexible, fully automated ChLIA processing. With the ability to process up to 140 tests per hour (assay dependent), the IDS i20 instrument is the latest addition to the well-established IDS i-device series, built on more than 50 years of experience in medical device design and innovation. The IDS i20 platform features new software offering a high degree of adaptability and scalability, along with a superior graphical user interface that meets the latest standards of ergonomics, usability and cybersecurity. Continuous loading of samples and reagents as well as the integrated cooling of ready-to-use reagent cartridges allow for non-stop operation of the system - maximizing efficiency and minimizing hands-on time.