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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

Alfa Wassermann Diagnostic Technologies

ACE Axcel

Company

Alfa Wassermann Diagnostic Technologies

Name of instrument

ACE Axcel

Email

info@alfawassermannus.com

City, State

West Caldwell, NJ

Phone

800-220-4488   

Website

http://www.alfawassermannus.com

Type of instrument

chemistry

List price/First year sold in U.S.

$41,875/2012

Targeted hospital bed size/Targeted test volume

—/daily: ~15–50 comprehensive metabolic panels and lipids

Company manufactures instrument

yes (also sold by McKesson, Henry Schein, Medline, AvMedical)

Other models in this family of analyzers

ACE Alera

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

Dimensions (H × W × D)/Instrument footprint

33 × 28 × 26 in./10 sq. ft.

Weight empty/Weight fully loaded

150 lbs./150 lbs.

No. of different measured assays onboard simultaneously

40 (200 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

15 (15 can be active simultaneously)

Test throughput per hour/Assay run time

165/—

No. of direct ion-selective electrode channels

3

Detection methods

photometry, potentiometry, turbidimetric homogeneous enzyme immunoassay

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

4 min./35 specimens per hr.

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

10 sec.

Fully automated microplate immunoassay system

Methodologies supported

Separation methodologies

Stat time until completion of a ß-hCG test

Stat time until completion of a cTn test

• Typical time delay from test order to aspiration of sample

Reagents refrigerated onboard/Reagents ready to use

yes (10°–14°C)/yes

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (open reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/no

Walkaway capability/Walkaway duration

yes/75 min. or 75 specimens or 248 tests

Design of sample-handling system

ring

Uses washable cuvettes/Uses disposable cuvettes

no/yes (can store up to 248 cuvettes)

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

3–200 µL

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

150 µL/53 µL/50 µL

Dedicated pediatric sample cup

no

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

Pierces caps on primary tubes

yes

Protects against probe collision

no

Detects clots/liquid level/short sample

no/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

yes (calibrants are not stored onboard)/yes

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

3 hrs./—/—/30 days/—

Automatic programmable start/Automatic programmable shutdown

no/no

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

yes/yes

Supports multiple QC lot numbers per analyte

yes

Waste management

automated collection onboard instrument

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, UPC, Codabar, Code 39, Code 128)/yes

Lab can control analyzer from remote computer

no

Instrument can diagnose its own malfunctions

yes (operator intervention required to order parts)

System malfunctions can be diagnosed via remote monitoring

no

UPS backup power supply

no

Data-management capability/LIS or EHR systems interfaced

onboard/CGM LabDaq, Clinisys, CGM SchuyLab, LabTrak, more

LIS interface provided/Bidirectional interface capability

no/yes (host query)

Modem servicing provided/Service engineer on-site response time

—/24 hrs.

Mean time between failures

240 days (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 15 min.; weekly: 20–30 min.; monthly: 30–40 min.

Maintenance records kept onboard for user/vendor

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

Maintenance training demonstration module onboard

no

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

yes (1 training slot)/4.5 days (at customer and vendor sites [depends on sales agreement])

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

no/—

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

yes (1 year)/—

Distinguishing features (supplied by company)

self-contained analyzer, closed-tube sampling, stat interrupt capability; onboard sample, reagent refrigeration; ready-to-use reagents, onboard reagent inventory management; integrated ISE module; no external water source or waste drainage; new vitamin D test provides results in 10 minutes

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