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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

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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

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.

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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

PixCell Medical

HemoScreen

Company

PixCell Medical

Name of analyzer

HemoScreen

Contact

Carmit Shpalter  

Email

info@pixcell-medical.com

City, State

Davie, FL

Phone

754-236-9694

Website

http://www.pixcell-medical.com

Analyzer application

diagnostic use

Dimensions of analyzer (H × W ×

11.8 × 6.9 × 10.2 in./0.56 sq. ft.

Country where analyzer was

Israel/Israel

First year analyzer was sold in U.S./Approximate No. of units installed in U.S.*

2018/—

First year analyzer sold outside

2016/—

Foreign locations where company

Europe, Asia (installed in Europe, Asia)

Human languages (other than

—

Analyzer list price

—

• Analyzer acquisition options

purchase, reagent rental agreement

Training included with purchase/Total time for basic training per operator

—

• Follow-up training available

—

Parameters that analyzer tests and reports

%&# eosinophils, %&# lymphocytes, %&# monocytes, %&# neutrophils, %&# basophils, Hb, Hct, MCH, MCHC, MCV, PLT, RBC, WBC

Types of testing FDA cleared or approved for analyzer

blood count analysis

Types of body fluids FDA cleared or approved for analysis on analyzer

whole blood

Analytical measurement range for body fluid

—

Precision for body fluid

—

Accuracy for body fluid

—

Automated differential performed for body fluids

yes (5-part differential)

Tests available for research use only

—

Differential methods used

digital microscopy and computer-vision algorithms

Analytical measurement range: • WBC count/RBC count

WBC: 0.25–95.0 × 103/µL/RBC: 1.0–8.8 × 106/µL 

Precision: • WBC count/RBC count

WBC: 4.0%/RBC: 1.5%

Accuracy: • WBC count/RBC count

—

Interfering substances: • WBC/RBC

no significant interference up to 50 mg/dL for bilirubin, 729 mg/dL for triglycerides/no significant interference up to 50 mg/dL for bilirubin, 729 mg/dL for triglycerides

• Hemoglobin/Platelets

no significant interference up to 50 mg/dL for bilirubin, 729 mg/dL for triglycerides/no significant interference up to 30 mg/dL for bilirubin, 729 mg/dL for triglycerides

• Hematocrit/Reticulocytes

no significant interference up to 50 mg/dL for bilirubin, 729 mg/dL for triglycerides/—

• Automated differential

—

Throughput: max. CBCs per hour/Max. CBCs with differentials per hour

20/10

• Max. No. of slides processed per hour if stainer included

—

FDA-cleared or -approved sample container types (besides potassium EDTA)

—

Min. specimen volume open mode/Closed mode/Microsample capability

40 µL/40 µL/yes

Types of patient data archived/Max. No. of archived patient data accessible when analyzer online

none/—

Analyzer performs delta checks

no

Parameters for which flags may appear

all CBC and differential parameters, pathologic flags, range flags, measurement condition flags, parameter warning, error flags

Analyzer recognizes and holds test results

no 

Scattergram display uses cell-specific color

no

Histogram display uses color with thresholds

no

LIS interface formats supported

HL7 version 2, HL7 version 3, POCT-1A

• Middleware interface

yes (can use Radiometer Aqure, Synlab MediPOC, Siemens Healthineers POCcelerator, Telcor, Abbott RALS, RelayMed, Orchard, SCC SoftLab, others)

• Information transferred to LIS via middleware or LIS interface

numeric results, flagged results

Analyzer transmits LOINC codes for results to LIS or middleware

yes

Lab automation system or workcells to which analyzer has a direct interface

Abbott Diagnostics, Telcor

Barcode symbologies read on specimen tube

Codabar, Code 39, Code 128

• Analyzer allows barcode placement per CLSI standard Auto02-A2

— (supports QR codes)

No. of onboard reagents required for standard specimen analysis

—

• Reagents ready to use/Reagent tracking method

—/barcode reader

Onboard diagnostics for troubleshooting

yes 

• Manufacturer can perform diagnostics via remote access

yes

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

one-year warranty/—

Notes

†also marketed by Thermo Fisher Scientific, Henry Schein, Medline

More products
in this guide

Alinity h-series
CELL-DYN Emerald†
CELL-DYN Emerald 22
CELL-DYN Emerald 22 Autoloader
GloCyte Automated Cell Counter for CSF
DxH 500 Hematology Analyzer
DxH 520 Hematology Analyzer
DxH 560 AL Hematology Analyzer
DxH 690T Hematology Analyzer
DxH 900 Workcell Automated Hematology Solution
ABX Micros 60
ABX Micros ES60
ABX Pentra 60C+
ABX Pentra XL80
Yumizen H2500
X100/X100HT with Full-Field Peripheral Blood Smear Application
XN-330, XN-430, XN-530
XN-350, XN-450, XN-550
XN Series† (XN-1000, XN-2000, XN-3100, XN-9100)