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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

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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

Gold Standard Diagnostics

Bolt

Company

Gold Standard Diagnostics

Name of instrument

Bolt

Email

gsd.sales@us.goldstandarddiagnostics.com

City, State

Davis, CA

Phone

530-759-8000  

Website

https://clinical.goldstandarddiagnostics.com/us

Type of instrument

immunoassay

Operational type/Model type

batch/benchtop

List price/First year sold in U.S.

—/2016

Targeted hospital bed size/Targeted test volume

—

Company manufactures instrument

yes (also sold by distribution partners)

Other models in this family of analyzers

Thunderbolt

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

—

Dimensions (H × W × D)/Instrument footprint

21.5 × 38.5 × 24 in. (width includes laptop)/6.42 sq. ft.

Weight empty/Weight fully loaded

60 lbs./110 lbs.

No. of different measured assays onboard simultaneously

open EIA platform (up to 12 with limit of two washes, nine reagents and common incubation temperature, plate frame type)

No. of user-definable (open chemistry) channels

—

Test throughput per hour/Assay run time

assay dependent (96 tests in throughput)/20 min.–4 hr. (avg. 2 hr.)

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

yes (96 tests per unit; 96 wells per microplate)

Methodologies supported

chemiluminescence, enzyme immunoassay

Separation methodologies

coated microwell

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

96/open reagent system

Reagents refrigerated onboard/Reagents ready to use

no (room temperature–40°C)/variable; reagent specific

Reagent lot tracking/Reagent inventory

yes/no

Reagent form/Reagents barcoded

liquid chemistry (open reagent system)/no

Separate reagent pack for each specimen/for each test run

no/yes

Walkaway capability/Walkaway duration

yes/avg. 120 min.

Design of sample-handling system

rack

Uses washable cuvettes/Uses disposable cuvettes

no/no

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

1–300 µL

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

25 µL/151 µL/150 µL

Dedicated pediatric sample cup

no

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/no

Pierces caps on primary tubes

no

Protects against probe collision

yes

Detects clots/liquid level/short sample

no/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

hemolysis, icterus, lipemia, clots not available

Dilutes patient samples onboard/Susceptibility to carryover

yes (can be programmed to perform dilutions prior to analysis)/assay specific

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 (recommended avg. frequency: per batch)

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

—/—/—/—/per batch

Automatic programmable start/Automatic programmable shutdown

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

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 (unspecified)/no

Lab can control analyzer from remote computer

no

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

no/yes (host query) 

Modem servicing provided/Service engineer on-site response time

yes/48 hrs.

Mean time between failures

— (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 5 min.; weekly: 15 min.; monthly: 20 min.

Maintenance records kept onboard for user/vendor

yes/some records (dye tests and calibrations)

Maintenance training demonstration module onboard

no

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

yes (No. of training slots client dependent)/4 hrs. (at customer or vendor site)

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

yes (at customer or vendor site)/yes (client dependent)

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

yes (1 year)/—

Distinguishing features (supplied by company)

open architecture: program any EIA or CLIA protocol, fully customizable with flexible, intuitive software; space saving: high capacity (96 samples) in 2 ft. × 2 ft. footprint; cost saving: low instrument price point with no routine consumables required

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