Webinars and Sponsored Roundtables — Register Now
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 Center, and Colin Murphy, CEO of mTuitive.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Tuesday, June 9, 2026, 1:00–2:00 PM ET
In this webinar, we will examine how immune recognition after allogeneic HCT can influence leukemia relapse and disease progression. The session will highlight the clinical relevance of HLA loss of heterozygosity (LOH), approaches used for its detection, and how LOH findings may support transplant strategies, including considerations for donor selection in subsequent transplantation.
Webinar presenter Alberto Cardoso Martins Lima, PhD, Clinical consulting scientist in histocompatibility,
specializing in allogeneic hematopoietic cell transplantation (HCT) at IGEN/AFIP São Paulo and CHC/UFPR in Curitiba, Brazil
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Wednesday, June 24, 2026, 12:00–1:00 PM ET
Hear an expert discuss the expanded clinical utility of HER2 IHC scoring in metastatic breast cancer and its impact on your practice
Webinar presenter Michelle Shiller, DO, AP, CP, MGP, FACP, Baylor University Medical Center.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Subspecialties
Interactive Product Guides
Product Spotlight
HemoSonics LLC
| Company | HemoSonics LLC |
|---|---|
| Instrument name/First year sold | Quantra Hemostasis Analyzer/2019 |
| Contact | Chris Gillespie |
| City, State | Durham, NC |
| Phone | 919-886-9674 |
| Website | |
| List price/Model type | —/portable, benchtop |
| No. of units in clinical use in U.S./Outside U.S. | >150/>150 (Europe, Japan, Hong Kong) |
| Composition of installs: Hospital lab/Reference lab/Other | 35%/0/65% (point of care [operating room, ICU, stat lab, more]) |
| Targeted daily, monthly, annual test volume | daily: 15–20; monthly: 1–200; annual: 1, 200–2, 400 |
| Operational type | random access, continuous random access |
| Country where analyzer designed/Manufactured | U.S./U.S. |
| Company manufactures instrument | yes |
| FDA-approved clotting-based tests | QPlus cartridge: clot time, clot time with heparinase, clot time ratio, clot stiffness, more; QStat cartridge: clot time, clot stability to lysis, clot stiffness, platelet contribution to clot stiffness, more |
| FDA-approved chromogenic tests | — |
| FDA-approved immunologic tests | — |
| Other FDA-approved tests | — |
| User-defined tests in clinical use | — |
| Tests in development or awaiting FDA 510(k) clearance | — |
| Methodologies supported | clot detection, sonic estimation of elasticity via resonance (SEER) sonorheometry |
| Number of different measured assays onboard simultaneously | QPlus cartridge: 6; QStat cartridge: 5 |
| Number of different assays programmed and calib. at one time | no calibration required |
| No. of user-definable (open) channels/No. active simultaneously | — |
| Factor assays require manual manipulation or dilutions | — |
| Test throughput per hour/Assay run time | 5–6 (25–36 tests in throughput)/7–60 min. (avg. 12.5 min.) |
| Design of sample-handling system | sealed room-temperature-stable cartridges accept a standard 3.2% citrate blue top tube, manually affixed to cartridge |
| Operates on whole blood or spun plasma | whole blood |
| Reagent type | self-contained single-use cartridges (lyophilized [reconstituted manually]) |
| Reagent barcode-reading capability | yes, for all tests |
| No. of reagent containers held onboard/Reagents ready to use | 1 cartridge/yes |
| Reagent lot tracking/Reagent inventory/Reagents refrigerated onboard | yes/no/no (20°–25°C) |
| Reagents, consumables loaded without interrupting testing | no |
| Instrument uses proprietary or third-party reagents | proprietary reagents |
| Maximum time same lot number of reagents can be used | — |
| Walkaway capability/Walkaway duration | yes/∼12.5 min. or 1 specimen or 5–6 tests |
| Min.–max. specimen volume that can be aspirated at one time | — |
| Min. sample volume required for PT/PTT/Factor VIII activity | single use cartridges, weekly cleaning cartridge, QC level 1 and 2 |
| Primary tube sampling supported/Pierces caps on primary tubes | yes/yes |
| Accommodates most standard tube sizes/Nonstandard sizes | yes/— |
| Sample barcode-reading capability/Autodiscrimination | yes/— |