Webinars and Sponsored Roundtables — Register Now

Tuesday, April 28, 2026, 12:00 PM–1:00 PM ET
Discover how next-day comprehensive genomic profiling (CGP) is possible with the Oncomine Comprehensive Assay Plus on the Genexus System—delivering both speed and accuracy.

Webinar presenters Jane Bayani, MHSc, PhD, Assistant Professor and Co-Director, Diagnostic Development, Ontario Institute for Cancer Research, Canada, and Nicola Normanno, MD, Scientific Director, IRCCS Romagnolo Institute for the Study of Tumors, Italy, and Morten Grauslund, PhD, Molecular Biologist, Department of Pathology, Rigshospitalet/Copenhagen University Hospital, Copenhagen, Denmark.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Thermo Fisher Scientific. For Research Use Only. Not for use in diagnostic applications. 

Thursday, April 30, 2026, 11:00 AM–12:00 PM ET
Hear an expert discuss how Memorial Sloan Kettering Cancer Center (MSKCC) is utilizing
the oncoReveal® Nexus 21-gene panel to redefine turnaround time and actionable insights
in cancer care. Dr. Ewalt shares a perceptive look at the clinical need for rapid, front-line NGS sequencing, and how a unique, purpose built targeted NGS panel (Pillar Biosciences’ oncoReveal Nexus 21 gene Panel) was developed, validated and implemented clinically by Memorial Sloan Kettering Cancer Center (MSK-REACT) to complement their current comprehensive genomic profiling (CGP) approach.

Webinar presenter Mark Ewalt, MD, Associate Medical Director for Laboratory Operations for Diagnostic Molecular Pathology in the Molecular Diagnostics Service, Department of Pathology and Laboratory Medicine, MSKCC.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

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

Thursday, May 28, 2026, 1:00–2:00 PM ET
This session is designed to improve understanding and application of recent updates to synoptic pathology reporting protocols such as the latest Reporting Template for Reporting Results of Biomarker Testing of Specimens from Patients with Carcinoma of the Breast. These changes reflect evolving clinical guidelines that directly influence diagnostic accuracy and treatment selection in breast cancer care.

Webinar presenters Thaer Khoury, MD, FCAP, Chair, Pathology and Laboratory Medicine, Roswell Park Comprehensive Cancer Cente, and Colin Murphy,  CEO of mTuitive.

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   graeme.mcneill@randox.com

Email

Kearneysville, WV

Phone

304-728-2890  

Website

https://www.randox.com

Type of instrument

chemistry

Operational type/Model type

discrete/benchtop

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 x 38 x 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

• Ion-selective electrode

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

• Basic metabolic panel

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

• 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

Approximate No. of tests per reagent set/Reagent type

200/self-contained single use

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

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

Analyzer requires dedicated water supply

yes (18 L/hr. consumption during operation)

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

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; stat sample capabilities; benchtop analyzer

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