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
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 presenters Michelle Shiller, DO, AP, CP, MGP, FACP, Baylor University Medical Center.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
August 2017—Techlab Inc. received FDA clearance for its E. Histolytica Quik Chek test, a rapid diagnostic test that specifically detects pathogenic E. histolytica and does not cross-react with nonpathogenic Entamoeba dispar.
August 2017—Qiagen has joined Cancer-ID, a public-private consortium of 36 partners from 13 countries that aims to establish standard protocols and clinical validation for blood-based biomarkers in lung and breast cancer.
July 2017—To define the current state of reagents and serological assay technology used to measure total human immunoglobulin E and IgE antibodies of defined allergen specificities in human blood, the Clinical and Laboratory Standards Institute published a revised document that focuses on IgE assay design and calibration, validation methods, quality assurance of assay reagents, quality control strategies, and clinical applications.
July 2017—Streck has signed distribution agreements with Anopoli Biomedical Systems, an Austrian distributor of life sciences, molecular diagnostics, and microarray products, and with Ngaio Diagnostics,
July 2017—Myriad Genetics has launched the EndoPredict test in the U.S. for patients with ER+ HER2- early stage breast cancer. EndoPredict is a second-generation test for assessing the 10-year risk of disease recurrence following surgery and for determining which patients can safely forgo adjuvant chemotherapy.
July 2017—Randox Quality Control launched a centralized platform for the management of daily quality control activities
July 2017—Becton Dickinson received 510(k) clearance from the FDA for its BD FACSVia, a flow cytometer system with a leucocount reagent assay used in residual white blood cell enumeration.
July 2017—Siemens Healthineers announced a strategic alliance with Relaymed to bring customers secure, cloud-based connectivity for Siemens DCA Vantage analyzer and Clinitek Status point-of-care instruments.
July 2017—Hemo Bioscience announced its MQC-CAT—a ready-to-use quality control product for manual column agglutination technology blood bank testing methods—has received FDA 510(k) clearance.
July 2017—Helomics and MDNA Life Sciences announced the commercial launch of MDNA’s liquid biopsy Prostate Mitomic Test in select U.S. markets. The proprietary test, which utilizes MDNA’s Mitomic Technology platform, uses the unique biological characteristics of mitochondrial DNA and is available in the clinical laboratories of Helomics.
