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Wednesday, September 23, 2026. 12 PM-1 PM ET
Roundtable presenters Dr. David Sacks MB, ChB, FRCPath, Chairman, Steering Committee National Glycohemoglobin Standardization Program (NGSP), and Priya Sivaraman, PhD, Senior Technical Product Manager, Tosoh Bioscience.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Thursday, September 24, 2026 11 AM-12 PM CT
This session explores the evolving role of RAS in precision oncology, from the biology of RAS mutations to the expanding landscape of targeted therapies. Through expert presentations, real-world case discussions, and interactive audience polling, participants will examine best practices for RAS biomarker testing across solid tumors, including lung, colorectal, and pancreatic cancers. The session will highlight practical considerations for tissue and liquid biopsy, strategies to address testing gaps, and the importance of multidisciplinary collaboration to ensure timely identification of patients who may benefit from RAS-targeted therapies.

Webinar presenters David Braxton, MD, Chief of Molecular Pathology Services, Hoag Family Cancer Institute & Hoag Memorial Hospital Presbyterian, and Carlos Becerra, MD, Research Director for Medical Oncology, Margaret Given Larkin Endowed Chair for Developmental Cancer Therapeutics, Hoag Memorial Hospital Presbyterian.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Wednesday, September 30, 2026. 1 PM-1:30 PM ET
Roundtable presenters John Longshore, PhD, Head of Scientific Affairs, Global Oncology Diagnostics, AstraZeneca, and Flora Berisha, MS, Executive Director, Global Head of Diagnostic Partnering and Development, Johnson & Johnson Innovative Medicine, and Mark D. Ewalt, MD, Associate Medical Director for Laboratory Operations, Diagnostic Molecular Pathology, Molecular Diagnostics Service, Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, and Isabel Preeshagul, DO, MBS, Thoracic Medical Oncologist, Memorial Sloan Kettering Cancer Center.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Tuesday, October 20, 2026 11 AM-12 PM ET
Hear experts review the biological and clinical significance of the HER2 expression continuum in breast tissue, providing a clearer understanding of how these variations might impact diagnosis, and discuss the emerging importance of documenting HER2-low and HER2-ultralow categories using a validated IHC assay.

Webinar presenters Keith Wharton, MD, PhD, Global Medical Affairs Leader–Pathology,
Roche Diagnostics Solutions, and Hannah Y. Wen, MD, PhD, Director, Breast Pathology Fellowship, Associate Team Leader, Breast Pathology Team, Attending Pathologist, Memorial Sloan Kettering Cancer Center.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Product Spotlight

Beckman Coulter

DxI 9000 Access Immunoassay Analyzer

Company

Beckman Coulter

Name of instrument

DxI 9000 Access Immunoassay Analyzer

Contact

Doug Lee   

Email

dylee@beckman.com

City, State

Brea, CA

Phone

800-526-3821   

Website

http://www.beckmancoulter.com

Type of instrument

immunoassay

List price/First year sold in U.S.

—/2023

Targeted hospital bed size/Targeted test volume

Company manufactures instrument

yes (also sold by McKesson, Henry Schein, Medline, Thermo Fisher Scientific)

Other models in this family of analyzers

Access 2, Unicel DxI 600, Unicel DxI 800

No. of units in clinical use in U.S./Outside U.S. (countries)

Dimensions (H × W × D)/Instrument footprint

63 × 79 × 41 in./22.5 sq. ft.

Weight empty/Weight fully loaded

1,785 lbs./—

No. of different measured assays onboard simultaneously

50 (50 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

0

Test throughput per hour/Assay run time

up to 450/8–50 min.

No. of direct ion-selective electrode channels

Detection methods

Stat time until completion/specimen throughput for Ion-selective electrode

Stat time until completion/specimen throughput for Ion-selective electrode basic metabolic panel

Stat time until completion/specimen throughput for Ion-selective electrode complete metabolic panel

Typical time delay from ordering stat test until aspiration of sample

Fully automated microplate immunoassay system

no

Methodologies supported

chemiluminescence

Separation methodologies

magnetic particle

Stat time until completion of a ß-hCG test

10 min.

Stat time until completion of a cTn test

12 min.

• Typical time delay from test order to aspiration of sample

16 sec.

Reagents refrigerated onboard/Reagents ready to use

yes (4°–10°C)/yes

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (closed reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/yes

Walkaway capability/Walkaway duration

yes/240 min. or 140 specimens

Design of sample-handling system

rack or direct track sampling when connected to automation

Uses washable cuvettes/Uses disposable cuvettes

no/yes

Min.–max. sample volume that can be aspirated at one time 

2–200 µL

Min. reaction volume/Min. specimen volume/Min. dead volume

5 µL/85 µL with direct sampling, 150 µL with standard sampling/80 µL

Dedicated pediatric sample cup

yes (dead volume: 150 µL)

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/no

Pierces caps on primary tubes

no

Protects against probe collision

no

Detects clots/liquid level/short sample

yes/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

hemolysis, icterus, lipemia, clots not available

Dilutes patient samples onboard/Susceptibility to carryover

yes (can be programmed to perform dilutions prior to analysis)/—

Automatic rerun capability

yes

Sample volume can be diluted to rerun out-of-linear-range high results

yes

Sample volume can be concentrated to rerun out-of-linear-range low results

no

Autocalibration/Multipoint calibration supported

no (calibrants are not stored onboard)/yes (recommended avg. frequency: 28 days)

Typical calibration frequency for ISE/therapeutic drugs/drugs of abuse/general chemistries/immunoassays

—/—/—/—/28 days

Automatic programmable start/Automatic programmable shutdown

no/no

Onboard real-time QC/Onboard software capability to review QC

no/yes

Supports multiple QC lot numbers per analyte

yes

Waste management

direct to drain

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128)/no

Lab can control analyzer from remote computer

yes 

Instrument can diagnose its own malfunctions

yes (instrument can order parts without operator intervention)

System malfunctions can be diagnosed via remote monitoring

yes

UPS backup power supply

no

Data-management capability/LIS or EHR systems interfaced

onboard/—

LIS interface provided/Bidirectional interface capability

yes (included in instrument price)/yes (broadcast download and host query)

Modem servicing provided/Service engineer on-site response time

yes/within 24 hrs.

Mean time between failures

— (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

weekly: < 15 min.; monthly: 7 min.

Maintenance records kept onboard for user/vendor

yes (includes audit trail of who replaced parts)/no

Maintenance training demonstration module onboard

yes

Training included with purchase/Avg. time for basic user training

yes (2 training slots)/3 days (at vendor site)

Advanced operator training/Extra charge for follow-up or advanced training

no/yes

Warranty provided/Cost of annual service contract (24 h/7 d)

yes (1 year)/—

Distinguishing features (supplied by company)

ZeroDaily Maintenance eliminates daily maintenance; less than 15 minutes of cleaning per week; PrecisionVision Technology uses multiple cameras with defined algorithms to detect processing errors in real time; SimpleSolve Onboard Guide provides instrument-guided troubleshooting with step-by-step instructions

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