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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

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Thursday, October 1, 2026 1 PM-2 PM ET
This presentation will explore the value of in-house CGP, offer insights into the benefits and drawbacks of incorporation, and provide information about important practical factors when considering in-house implementation of CGP.

Webinar presenter Allison M. Cushman-Vokoun, MD, PhD, FCAP, Medical Director, Molecular Diagnostics and Personalized Medicine Laboratory, Director, Division of Diagnostic Molecular Pathology and Human Genetics, Henry F. Krous Professor of Pathology, University of Nebraska Medical Center

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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

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Roche.

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Tuesday, November 3, 2026 1 PM-2 PM ET
Hear an expert discuss the challenges of detecting NRG1 fusions and how RNA-based testing can support more comprehensive fusion identification in clinical practice.

Webinar presenter Benjamin Weinberg, MD, Associate Professor of Medicine and Attending Physician
specializing in gastrointestinal medical oncology

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Diaceutics.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Product Spotlight

Tosoh Bioscience

AIA-360

Company

Tosoh Bioscience

Name of instrument

AIA-360

Email

info.diag.am@tosoh.com

City, State

Grove City, OH

Phone

800-248-6764  

Website

https://www.diagnostics.us.tosohbioscience.com

Type of instrument

immunoassay

Operational type/Model type

continuous random access/benchtop

List price/First year sold in U.S.

—/2004

Targeted hospital bed size/Targeted test volume

—/monthly: < 500

Company manufactures instrument

yes

Other models in this family of analyzers

AIA-900, AIA-2000

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

~600/> 7,000 (worldwide)

Dimensions (H × W × D)/Instrument footprint

21 × 16 × 16 in./2.1 sq. ft.

Weight empty/Weight fully loaded

61 lbs./—

No. of different measured assays onboard simultaneously

25 (25 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

—

Test throughput per hour/Assay run time

36/20 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 basic metabolic panel

—

Stat time until completion/specimen throughput for complete metabolic panel

—

Typical time delay from ordering stat test until aspiration of sample

—

Fully automated microplate immunoassay system

—

Methodologies supported

fluorescence enzyme immunoassay (FEIA)

Separation methodologies

—

Stat time until completion of a ß-hCG test

20 min.

Stat time until completion of a cTn test

20 min.

• Typical time delay from test order to aspiration of sample

—

Approximate No. of tests per reagent set/Reagent type

100 (20 tests per tray)/unit dose test cup

Reagents refrigerated onboard/Reagents ready to use

no/yes

Reagent lot tracking/Reagent inventory

yes/no

Reagent form/Reagents barcoded

dry chemistry (closed reagent system)/yes

Separate reagent pack for each specimen/for each test run

yes/—

Walkaway capability/Walkaway duration

yes/58 min. or 25 specimens or 25 tests/assays

Design of sample-handling system

carousel

Uses washable cuvettes/Uses disposable cuvettes

no/no

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

10–100 µL

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

10 µL/110 µL/100 µL

Dedicated pediatric sample cup

no

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/—

Pierces caps on primary tubes

no

Protects against probe collision

—

Detects clots/liquid level/short sample

yes/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

—

Dilutes patient samples onboard/Susceptibility to carryover

no/none

Automatic rerun capability

no

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

no

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

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

—/—/—/—/90 days most assays

Automatic programmable start/Automatic programmable shutdown

no (5 min. start-up time)/no

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

no/no

Supports multiple QC lot numbers per analyte

—

Waste management

automated collection onboard instrument

Sample barcode-reading capability/Autodiscrimination

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

Lab can control analyzer from remote computer

no

Instrument can diagnose its own malfunctions

no

System malfunctions can be diagnosed via remote monitoring

—

UPS backup power supply

yes

Data-management capability/LIS or EHR systems interfaced

Tosoh 501RP+/—

LIS interface provided/Bidirectional interface capability

no/no

Modem servicing provided/Service engineer on-site response time

—

Mean time between failures

888 days (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 5 min.

Maintenance records kept onboard for user/vendor

no/no

Maintenance training demonstration module onboard

no

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

yes/2 days (at customer site)

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

—

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

yes (1 year)/—

Distinguishing features (supplied by company)

unit dose test cup; dry reagent, no premixing or reagent preparation; immunoassay method free from biotin interference; compact size, broad menu with fast results; 90-day calibration stability for most assays

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