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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

Randox Laboratories

RX imola

Company

Randox Laboratories

Name of instrument

RX imola

Contact

Graeme McNeill   

Email

graeme.mcneill@randox.com

City, State

Kearneysville, WV

Phone

304-728-2890   

Website

http://www.randox.com

Type of instrument

chemistry

List price/First year sold in U.S.

—/2006

Targeted hospital bed size/Targeted test volume

75/daily: > 750; monthly: > 22,500; annual: > 270,000

Company manufactures instrument

yes

Other models in this family of analyzers

RX misano, RX monaco, RX daytona +, RX modena

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

34/> 1,000 (> 120 countries)

Dimensions (H × W × D)/Instrument footprint

27 × 38 × 23 in./44.28 sq. ft.

Weight empty/Weight fully loaded

331 lbs./340 lbs.

No. of different measured assays onboard simultaneously

60 (60 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

15 (0 can be active simultaneously)

Test throughput per hour/Assay run time

560, including ISE (50 tests in throughput)/5–10 min. (avg. 6 min.)

No. of direct ion-selective electrode channels

3

Detection methods

potentiometry

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

13 min. 15 sec./80 specimens per hr.

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

13 min. 43 sec./80 specimens per hr.

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

13 min. 15 sec./67 specimens per hr.

Typical time delay from ordering stat test until aspiration of sample

30 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 (8°–15°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/no

Walkaway capability/Walkaway duration

yes/70 min. or 40 specimens or 10 tests

Design of sample-handling system

ring

Uses washable cuvettes/Uses disposable cuvettes

yes (can store up to 90 cuvettes)/no

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

1.5–35 µL

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

150 µL/1.5–35 µL/150 µL

Dedicated pediatric sample cup

yes (dead volume: 100 µL)

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

Pierces caps on primary tubes

no

Protects against probe collision

yes

Detects clots/liquid level/short sample

yes/yes/no

Detection or quantitation for hemolysis, icterus, lipemia, clots

detection and quantitation for hemolysis, icterus, lipemia; clots not available

Dilutes patient samples onboard/Susceptibility to carryover

yes (can be programmed to perform dilutions prior to analysis)/no carryover

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

yes

Autocalibration/Multipoint calibration supported

no (calibrants can be stored onboard)/yes (recommended avg. frequency: 14 days)

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

1 day/7 days/7 days/14 days/28 days

Automatic programmable start/Automatic programmable shutdown

yes (9 min. warm-up time)/yes

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

—/yes

Supports multiple QC lot numbers per analyte

yes

Waste management

direct to drain

Sample barcode-reading capability/Autodiscrimination

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

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

onboard/—

LIS interface provided/Bidirectional interface capability

yes (included in instrument price)/yes (host query)

Modem servicing provided/Service engineer on-site response time

no/within 24 hrs.

Mean time between failures

2 per 3 years (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 5 min.; weekly: 15 min.; monthly: 1 hr.

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 (1 training slot)/3 days (at customer site)

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

yes (at customer site)/yes

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

yes (1 year)/—

Distinguishing features (supplied by company)

large and extensively dedicated test menu; stat sample capabilities; benchtop analyzer

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