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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

Diatron MI

Pictus 500 (P500)

Company

Diatron MI

Name of instrument

Pictus 500 (P500)

Contact

Frank Matuszak  

Email

frank.matuszak@diatron.com

City, State

Medley, FL

Phone

833-228-7931  

Website

https://www.diatron.com

Type of instrument

chemistry

Operational type/Model type

batch, random access, continuous random access, discrete/benchtop

List price/First year sold in U.S.

$42,860/2016

Targeted hospital bed size/Targeted test volume

20–100/daily: 500–2,500; monthly: 15,000–75,000; annual: 182,500–912,500

Company manufactures instrument

yes

Other models in this family of analyzers

Pictus 700 (P700)

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

> 40/≤ 200 (Europe, Latin America, Africa, Middle East, Asia)

Dimensions (H × W × D)/Instrument footprint

24.4 × 35.4 × 26 in./6.4 sq. ft.

Weight empty/Weight fully loaded

253 lbs./271 lbs.

No. of different measured assays onboard simultaneously

72 (999 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

Test throughput per hour/Assay run time

500/30–1,200 sec. (avg. 300 sec.)

No. of direct ion-selective electrode channels

3

Detection methods

photometry, potentiometry 

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

2 min./60 specimens per hr.

Stat time until completion/specimen throughput for basic metabolic panel

7.5 min./45 specimens per hr.

Stat time until completion/specimen throughput for complete metabolic panel

9 min./25 specimens per hr.

Typical time delay from ordering stat test until aspiration of sample

24 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

50–200 per set, 400–1,800 per pack/self-contained multiuse, open reagent system

Reagents refrigerated onboard/Reagents ready to use

yes (8°±2°C)/yes

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (open reagent system)/no

Separate reagent pack for each specimen/for each test run

no/no

Walkaway capability/Walkaway duration

yes/180 min. or 95 specimens or 1,200 tests/assays

Design of sample-handling system

rack

Uses washable cuvettes/Uses disposable cuvettes

yes/yes (can store up to 80 cuvettes)

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

2–100 µL

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

180 µL/22 μL/100 μL

Dedicated pediatric sample cup

yes (dead volume: 20 μL)

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/no

Pierces caps on primary tubes

yes

Protects against probe collision

yes

Detects clots/liquid level/short sample

yes/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

detection for clots; hemolysis, icterus, lipemia not available

Dilutes patient samples onboard/Susceptibility to carryover

yes (can be programmed to perform dilutions prior to analysis)/30 parts per million

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

yes (calibrants can be stored onboard)/yes (recommended avg. frequency: 7 days)

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

8 hrs./—/7 days/14 days/14 days

Automatic programmable start/Automatic programmable shutdown

no/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 or direct to drain

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, UPC, Codabar, Code 39, Code 128)/no

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/AP Vision, Medicus, Schuyler, LabTrack, CGM LabDaq, Medytox

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/48 hrs.

Mean time between failures

1 per year (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 30 min.; weekly: 1 hr.; monthly: 2 hrs.

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 (2 training slots)/3 days (at customer site)

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

yes (at customer or vendor site)/yes

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

yes (1 year)/$5,500

Distinguishing features (supplied by company)

uninterrupted workflow; Windows-based, intuitive, user-friendly software; high-quality components for long stability and result reliability

Note

all information listed was provided to CAP TODAY in 2025; company did not provide updated information by 2026 entry deadline

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