Webinars and Sponsored Roundtables — Register Now

Tuesday, November 3, 2026, 1 PM-2 PM ET
Hear an expert discuss the challenges of detecting NRG1 fusions and how RNA-based testing can support more comprehensive fusion identification in clinical practice.

Webinar presenter Benjamin Weinberg, MD, Associate Professor of Medicine and Attending Physician
specializing in gastrointestinal medical oncology

CAP TODAY does not endorse any of the products or services named within. The webinar is made possible by a special educational grant from Diaceutics.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Tuesday, November 10, 2026, 1 PM-2 PM ET
Join us for a session to help improve diagnostic accuracy in your practice when scoring HER2 IHC 0 with faint, incomplete membrane staining in ≤10% of tumor cells vs IHC 0 with no membrane staining detected in patients with mBC.

Webinar presenter Jeffrey Gregg, MD, University of Nevada

CAP TODAY does not endorse any of the products or services named within. This program is being sponsored by Daiichi Sankyo, Inc. and AstraZeneca. The speaker is being compensated for the presentation. The program is not CME accredited and may not be used for CME accreditation.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Monday, November 16, 2026, 12:30 PM-2 PM ET
Hear experts discuss a multidisciplinary approach to oncopathology for HER2
assessments for solid tumors in the absence of a companion diagnostic.

Webinar presenters Funda Meric-Bernstam, MD, Chair, Department of Investigational Cancer Therapeutics Medical Director, Institute for Personalized Cancer Therapy, The University of Texas MD Anderson Cancer Center, Houston, Texas, and Emina E. Torlakovic, MD, PhD, College of Medicine, University of Saskatchewan, Canadian Biomarker Quality Assurance, Saskatoon, Saskatchewan, Canada, and Carol Cheung, MD, PhD, JD, FRCPC, Deputy Director, Canadian Biomarker Quality, Assurance—Programme canadien d’assurance de la qualité des biomarqueurs

CAP TODAY does not endorse any of the products or services named within. This program is being sponsored by Daiichi Sankyo, Inc. and AstraZeneca. The speaker is being compensated for the presentation. The program is not CME accredited and may not be used for CME accreditation.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

Wednesday, December 9, 2026, 12 PM-1 PM ET
Hear an expert pathologist discuss the role of HER2 IHC testing and scoring in solid tumors including endometrial, ovarian, cervical, bladder, non-small cell lung, colorectal, and biliary cancers

Webinar presenter Michelle Shiller, DO, MSPT, Baylor Sammons Cancer Center; Fulgent Genetics; Texas Cancer Interception Institute

CAP TODAY does not endorse any of the products or services named within. This program is intended for US healthcare professionals. This program is being sponsored by AstraZeneca. The speaker is being compensated for the presentation. The program is not CME accredited and may not be used for CME accreditation.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

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Anchor Molecular releases MSI FFPE controls

July 2026—Anchor Molecular has launched its MSI FFPE controls designed to support microsatellite instability assay development, validation, and routine quality control applications. Each product contains 10-µm FFPE tissue slices embedded with cellular DNA exhibiting either microsatellite stable (MSS) status or microsatellite instability-high (MSI-H) status.

Seegene releases CE-marked Allplex MDRO assay

July 2026—Seegene launched its new antimicrobial resistance testing product, the Allplex MDRO assay. The assay, which is CE marked under the EU in vitro diagnostic regulation, is designed to identify key multidrug-resistant pathogens and associated resistance genes in a single run and can support same-day reporting, depending on laboratory workflow.

Sysmex introduces next-gen XR-Series hematology solution

July 2026—Sysmex America has introduced the XR-Series, a hematology solution designed to help laboratories deliver fast, reliable results while maintaining efficient workflows. The next-generation XR-Series builds on the capabilities of the XN-Series, adding higher throughput, enhanced analytics, and complementary solutions that aim to streamline daily laboratory operations.

Roche introduces Cobas MPX-E assay for HIV, hepatitis

July 2026—Roche introduced the Cobas MPX-E assay, a qualitative in vitro test for the detection and discrimination of HIV 1 and 2 and hepatitis C, B, and E viruses, in countries accepting the CE mark. By identifying these pathogens simultaneously, the assay aims to help laboratories streamline their operations while enhancing the safety of blood and blood products for patients.

QuidelOrtho completes acquisition of Lex Diagnostics

July 2026—QuidelOrtho has completed the acquisition of Lex Diagnostics for about $100 million in cash. The acquisition follows the FDA 510(k) clearance and CLIA waiver of the Lex Velo molecular diagnostics platform in February.

CareDx to acquire Naveris

July 2026—CareDx has entered into a definitive agreement to acquire Naveris for $160 million up front plus up to $100 million in additional payments tied to revenue milestones. Naveris is a precision oncology diagnostics company with a Medicare-reimbursed, blood‑based monitoring test for cancers caused by viral infections.

FDA-approved, at-home ColoSense test

July 2026—Labcorp announced that ColoSense, an FDA-approved, at-home test for colorectal cancer screening, is now available for adults ages 45 to 85 who are at average risk for developing CRC. The test uses RNA-based technology to detect biomarkers associated with colorectal cancer and advanced adenomas.

CHOP, Labcorp collaborate to accelerate access to pediatric diagnostics

July 2026—Labcorp and Children’s Hospital of Philadelphia are collaborating to advance the discovery, development, and availability of specialized pediatric diagnostics. CHOP and Labcorp will create a joint pediatric diagnostics innovation pipeline in which the organizations will identify, develop, and expand new tests and technologies, with the aim of streamlining the path from discovery to national availability.