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
Siemens Healthineers
| Company | Siemens Healthineers |
|---|---|
| Instrument name | CS-2500 System |
| Contact | Laura Oversmith |
| City State | Tarrytown, NY |
| Phone | 914-631-8000 |
| First year sold | 2016 |
| Website | |
| List price/Model type | $155, 000/benchtop |
| Dimensions (H × W × D)/Weight/Instrument footprint | 27 × 30.6 × 35.2 in./242.5 lbs./7.5 sq. ft. |
| No. of units in clinical use in U.S./Outside U.S. | >500/>2, 000 (worldwide) |
| Composition of installs: Hospital lab/Reference lab/Other | — |
| Targeted daily, monthly, annual test volume | daily: 25–300 |
| Operational type | continuous random access |
| Country where analyzer designed/Manufactured | Japan/Japan |
| Company manufactures instrument | no (manufactured by Sysmex) |
| FDA-approved clotting-based tests | PT, APTT, fibrinogen, factors II, V, VII, VIII, IX, X, XI and XII, protein C, lupus screen, lupus confirm, factor V Leiden, thrombin time, batroxobin time |
| FDA-approved chromogenic tests | antithrombin, protein C, Innovance free protein S antigen, plasminogen, Innovance heparin, factor VIII chromogenic, alpha-2-antiplasmin, Innovance anti-Xa |
| FDA-approved immunologic tests | Innovance VWF activity, VWF antigen, Innovance D-dimer |
| Other FDA-approved tests | — |
| User-defined tests in clinical use | platelet aggregation RUO, factor XIII chromogenic RUO |
| Tests in development or awaiting FDA 510(k) clearance | — |
| Methodologies supported | clot detection, optical; turbidimetric; chromogenic; immunologic (immunoturbidimetric) |
| Number of different measured assays onboard simultaneously | 60 |
| Number of different assays programmed and calib. at one time | 60 |
| No. of user-definable (open) channels/No. active simultaneously | 80, 000/60 |
| Factor assays require manual manipulation or dilutions | — |
| Test throughput per hour/Assay run time | 180 (2 tests in throughput)/1–10 min. (avg. 5 min.) |
| Design of sample-handling system | 10-tube position sample rack with a maximum of 5 × racks |
| Operates on whole blood or spun plasma | spun plasma |
| Reagent type | self-contained single-use vials; open reagent system (liquid, lyophilized [reconstituted manually]) |
| Reagent barcode-reading capability | yes, for all tests |
| No. of reagent containers held onboard/Reagents ready to use | 45/variable (reagent specific) |
| Reagent lot tracking/Reagent inventory/Reagents refrigerated onboard | yes/yes/yes (10°C ± 2°C) |
| Reagents, consumables loaded without interrupting testing | yes (reagents and consumables) |
| Instrument uses proprietary or third-party reagents | user’s option (same capabilities when third-party reagents used) |
| Maximum time same lot number of reagents can be used | 18 months |
| Walkaway capability/Walkaway duration | yes/50 specimens or up to 500 tests |
| Min.–max. specimen volume that can be aspirated at one time | 5–500 µL |
| Min. sample volume required for PT/PTT/Factor VIII activity | 50 µL/50 µL/5 µL (standard) |
| Types of disposables used | reaction cuvettes, CA clean I, CA clean II |
| Primary tube sampling supported/Pierces caps on primary tubes | yes/yes |
| Accommodates most standard tube sizes/Nonstandard sizes | yes/yes |
| Sample barcode-reading capability/Autodiscrimination | yes (Interleaved 2 of 5, Code 39, Code 128)/yes |
| Auto tracks product volume/Measures number of tests remaining | yes/yes |
| Short sample detection | yes |
| Clot detection as preanalytical variable in plasma sample | yes |
| Auto detects adequate reagents for aspiration or analysis | yes (aspiration and analysis) |
| Detection or quantitation for hemolysis, turbidity, icterus, lipemia | detection and quantitation for hemolysis, turbidity, icterus, lipemia |
| Dilutes patient samples onboard | yes |
| Automatic rerun capability/Auto reflex testing capability | yes/yes |
| Lag time during which hypercoagulable sample not detected | yes (PT: 7 seconds; PTT: 15 seconds) |
| User can adjust reagent volumes/Sample volumes | yes/yes |
| User can adjust No. of reagents/Sources of reagents | yes/yes |
| User can adjust incubation times/Reading times | yes/yes |
| Autocalibration/Calibrants stored onboard | yes/yes |
| Multipoint calibration supported/Recommended frequency | yes/6 months, per regulatory guidelines |
| • PT alone | <5 minutes/180 specimens |
| • PT, PTT | <5 minutes/90 specimens |
| • Fibrinogen | <5 minutes/180 specimens |
| • Factor VIII activity assay | <5 minutes/— |
| • D-dimer | <5 minutes/90 specimens |
| Time delay from ordering stat to aspiration of sample | <1 minute |
| How labs get LOINC codes for results | website |
| Onboard real-time QC/Onboard software capability to review QC | yes/yes |
| Information that can be barcode-scanned on instrument | operator identifier, specimen identifier, reagent lot No., reagent vial ID, reagent expiry |
| Compatible with laboratory automation systems | no |
| Data-management capability/LIS or EHR systems interfaced | onboard/most major vendors |
| Interface supplied by instrument vendor | contract dependent |
| Results transferred to LIS as soon as test time complete | yes |
| Bidirectional interface capability | yes (host query) |
| Remote servicing provided/UPS backup power supply | yes/yes |
| Instrument connections to transfer information | data-management system, which in turn connects to LIS or EHR; directly to LIS or EHR; directly to lab automation system; commercial middleware (most major companies) |
| Interface standards supported | ASTM 1394-91, ASTM 1381, HL7, CA-1000 protocol, CA-1500 protocol |
| Information transferred to data-management software | device unique identifier, operator ID, patient ID, specimen ID, result, QC identifier, PSI checks |
| Avg. time for basic user training | 2 days (at customer site), some self-study virtual training required |
| Approximate scheduled maintenance time | daily: <5 minutes; weekly: <10 minutes; monthly: <10 minutes |
| Maintenance records kept onboard | yes |
| Warranty with purchase/Annual service contract cost (24/7) | yes/— (cost dependent on contract) |
| Distinguishing features (supplied by company) | simultaneous multiwavelength detection and PSI technology designed to ensure high-quality first-run results; user-friendly software on Windows 10; tilted reagent vials for efficiency; for multisite patient monitoring, with sample result traceability for in-depth audit capabilities |