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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

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

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

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

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

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

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.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

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

Abbott Point of Care

i-STAT 1 analyzer

Company

Abbott Point of Care

Name of instrument

i-STAT 1 analyzer

Contact

Jeff Abney

Email

jeff.abney@abbott.com

City, State

Princeton, NJ

Phone

609-454-9000  

Website

https://www.pointofcare.abbott/us/en/home

Type of instrument

combination chemistry/immunoassay

Operational type/Model type

discrete/handheld

List price/First year sold in U.S.

—/2000

Targeted hospital bed size/Targeted test volume

all/—

Company manufactures instrument

yes (also sold by McKesson, Henry Schein, Medline, Cardinal, Concordance, others)

Other models in this family of analyzers

i-STAT Alinity

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

> 30,000/> 10,000 (Europe, Latin America, Africa, Middle East, Asia Pacific)

Dimensions (H × W × D)/Instrument footprint

9.25 × 3 × 2.85 in./< 1 sq. ft.

Weight empty/Weight fully loaded

< 2 lbs./< 2 lbs.

No. of different measured assays onboard simultaneously

—

No. of user-definable (open chemistry) channels

—

Test throughput per hour/Assay run time

—/2–15 min.

No. of direct ion-selective electrode channels

up to 26

Detection methods

potentiometry, amperometry, conductometry

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

2 min./20–25

Stat time until completion/specimen throughput for basic metabolic panel

2 min./20–25

Stat time until completion/specimen throughput for complete metabolic panel

—

Typical time delay from ordering stat test until aspiration of sample

none

Fully automated microplate immunoassay system

yes (up to 26 tests per unit)

Methodologies supported

potentiometry, amperometry, conductometry

Separation methodologies

none necessary

Stat time until completion of a ß-hCG test

—

Stat time until completion of a cTn test

10 min.

• Typical time delay from test order to aspiration of sample

none

Approximate No. of tests per reagent set/Reagent type

—/self-contained single use

Reagents refrigerated onboard/Reagents ready to use

no/—

Reagent lot tracking/Reagent inventory

no/no

Reagent form/Reagents barcoded

dry chemistry, liquid chemistry (closed reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/no

Walkaway capability/Walkaway duration

yes/2–10 min. or 1 specimen or up to 13 tests

Design of sample-handling system

—

Uses washable cuvettes/Uses disposable cuvettes

no/no

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

17–95 µL

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

—

Dedicated pediatric sample cup

no

Primary tube sampling

no

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

no/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

detection for hemolysis, icterus, lipemia, clots

Dilutes patient samples onboard/Susceptibility to carryover

no/—

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

yes (calibrants are not stored onboard)/yes (recommended avg. frequency: each test)

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

—/—/—/each test/each test

Automatic programmable start/Automatic programmable shutdown

yes/yes

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

yes/yes

Supports multiple QC lot numbers per analyte

yes

Waste management

manually by user

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128, EAN-8, EAN-13)/—

Lab can control analyzer from remote computer

yes

Instrument can diagnose its own malfunctions

yes (operator intervention required to order parts)

System malfunctions can be diagnosed via remote monitoring

yes

UPS backup power supply

no

Data-management capability/LIS or EHR systems interfaced

optional add-on/—

LIS interface provided/Bidirectional interface capability

yes (additional cost)/no

Modem servicing provided/Service engineer on-site response time

—/— (product replacement within 24 hrs.)

Mean time between failures

— (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

—

Maintenance records kept onboard for user/vendor

—

Maintenance training demonstration module onboard

—

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

—/4 hrs. (at customer site)

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

yes (at customer site)/no

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

yes (1 year)/—

Distinguishing features (supplied by company)

handheld portable analyzer; unit use system can perform chemistry, blood gas, cardiac marker, hematology, and coagulation tests; CLIA-waived tests, including glucose and creatinine; uses 2–3 drops of whole blood or plasma

Note

all information listed was provided to CAP TODAY in 2025; company did not provide updated information by 2026 entry deadline

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