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

Sebia

dIFine P30 Processor

Company

Sebia

Name of instrument

dIFine P30 Processor

Contact

Marketing  

Email

marketing@zeusscientific.com

City, State

Branchburg, NJ

Phone

908-526-3744  

Website

https://www.sebia.com

Type of instrument

immunoassay

Operational type/Model type

batch/benchtop

List price/First year sold in U.S.

Targeted hospital bed size/Targeted test volume

annual: > 5, 000

Company manufactures instrument

no

Other models in this family of analyzers

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

Dimensions (H × W × D)/Instrument footprint

29.1 x 34.6 x 33.1 in./8 sq. ft.

Weight empty/Weight fully loaded

220 lbs./—

No. of different measured assays onboard simultaneously

30 (30 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

Test throughput per hour/Assay run time

assay dependent/—

No. of direct ion-selective electrode channels

Detection methods

• Ion-selective electrode

• Basic metabolic panel

• Complete metabolic panel

Typical time delay from ordering stat test until aspiration of sample

Fully automated microplate immunoassay system

no

Methodologies supported

fluorescence

Separation methodologies

IFA slide well washing

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

80–240/open reagent system

Reagents refrigerated onboard/Reagents ready to use

no/yes

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (open reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/yes

Walkaway capability/Walkaway duration

yes/240 specimens or 30 tests

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 

10–1, 000 µL

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

Dedicated pediatric sample cup

yes

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

no

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)/—

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

Analyzer requires dedicated water supply

no

Autocalibration/Multipoint calibration supported

no (calibrants are not stored onboard)/no

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

Automatic programmable start/Automatic programmable shutdown

no/no

Supports multiple QC lot numbers per analyte

no

Waste management

automated collection onboard instrument

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, 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

no

Data-management capability/LIS or EHR systems interfaced

onboard/yes

LIS interface provided/Bidirectional interface capability

no/yes (host query)

Modem servicing provided/Service engineer on-site response time

no/within 24 hrs.

Mean time between failures

— (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: performed automatically; weekly: 5 min.; monthly: 10 min.

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 site)/no

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

yes (1 year)/—

Distinguishing features (supplied by company)

processes up to 240 samples and 30 IFA slides with a small footprint; fully automated–performs dilution, incubation, washing, mounting, and coverslipping; reliable traceability of samples, reagents, and slides owing to integrated barcode readers

More products
in this guide

Alinity ci-series
DxI 9000 Access Immunoassay Analyzer
Agility Automated ELISA System
Envoy 500/Envoy 500+ Chemistry Analyzer
AIX1000 Agglutination Instrument
Yumizen C1200
Yumizen C560
VITROS 4600 Chemistry System
VITROS XT 7600 Integrated System
cobas 6000 analyzer series
cobas 8000 modular analyzer series
cobas pro integrated solutions
IMMULITE 2000 XPi Immunoassay System
Phadia 250 Laboratory System
QUANTA-Lyser 3000