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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

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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

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Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Subspecialties

Interactive Product Guides

Product Spotlight

bioMérieux

VIDAS 3

Company

bioMérieux

Name of instrument

VIDAS 3

Contact

Kara Hardin  

Email

kara.hardin@biomerieux.com

City, State

Salt Lake City, UT

Phone

800-682-2666  

Website

https://www.biomerieux-usa.com

Type of instrument

immunoassay

Operational type/Model type

batch, random access, continuous random access/benchtop

List price/First year sold in U.S.

—/2015

Targeted hospital bed size/Targeted test volume

—

Company manufactures instrument

yes

Other models in this family of analyzers

—

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

> 500/—

Dimensions (H × W × D)/Instrument footprint

24 × 29.5 × 25.5 in./5.2 sq. ft.

Weight empty/Weight fully loaded

154 lbs./—

No. of different measured assays onboard simultaneously

12 (several different lots of assays can be stored at one time)

No. of user-definable (open chemistry) channels

—

Test throughput per hour/Assay run time

up to 36/assay dependent

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

no

Methodologies supported

enzyme-linked fluorescent assay (ELFA) technology

Separation methodologies

—

Stat time until completion of a ß-hCG test

25 min. (measures intact molecule)

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

30–60 per kit/self-contained single use

Reagents refrigerated onboard/Reagents ready to use

no/yes

Reagent lot tracking/Reagent inventory

yes/—

Reagent form/Reagents barcoded

liquid chemistry (closed reagent system)/yes

Separate reagent pack for each specimen/for each test run

yes/yes

Walkaway capability/Walkaway duration

yes/27 specimens or 12 tests

Design of sample-handling system

rack

Uses washable cuvettes/Uses disposable cuvettes

no/—

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

100–300 µL

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

100 µL/100 µL/125 µL for aliquot tubes

Dedicated pediatric sample cup

yes

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

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

Automatic rerun capability

no

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 (recommended avg. frequency: 14, 28, or 56 days)

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

—/—/—/—/every 14, 28, or 56 days

Automatic programmable start/Automatic programmable shutdown

yes (5 min. warm-up time)/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 or 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

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

yes

Data-management capability/LIS or EHR systems interfaced

onboard/Oracle Health, SCC Soft Computer, Meditech, Epic, more

LIS interface provided/Bidirectional interface capability

yes (additional cost)/yes (broadcast download and host query)

Modem servicing provided/Service engineer on-site response time

no/< 24 hrs.

Mean time between failures

> 1 year (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

weekly: 10–15 min.

Maintenance records kept onboard for user/vendor

yes/no

Maintenance training demonstration module onboard

no

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

yes/— (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)

specialty menu of critical care (mild traumatic brain injury, acute kidney injury, sepsis, thrombosis), infectious disease (MMRV, Lyme, C. difficile, H. pylori, toxoplasmosis, CMV), and hormone (hCG, progesterone, estradiol, LH, FSH) assays; easy-to-use benchtop immunoassay system with single-test, ready-to-use reagent format; mean time between failure > 370 days

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