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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. 

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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.

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 Cente, and Colin Murphy,  CEO of mTuitive.

Moderated by: Bob McGonnagle, Publisher, CAP TODAY

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Interactive Product Guides

Marketplace

Diasorin C. auris assay launched in countries accepting the CE mark

April 2025—Diasorin announced the launch of its Simplexa C. auris Direct kit in all countries that accept the CE mark. The real-time polymerase chain reaction assay is used for the direct in vitro qualitative detection of C. auris DNA from a composite swab of the axilla and groin from patients suspected of C. auris colonization. The assay detects all six C. auris clades identified worldwide. Results are available in less than two hours on the Liaison MDX.

Advanced Instruments acquires Nova Biomedical

April 2025—Advanced Instruments, a subsidiary of Patricia Industries, announced the execution of a definitive agreement to acquire Nova Biomedical. Following the close of the transaction, Advanced Instruments and Nova Biomedical will merge and operate under the Nova Biomedical name. Byron Selman, president and CEO of Advanced Instruments, will lead the combined business, while Nova Biomedical founding shareholders Frank Manganaro, CEO, and Dr. Chung-Chang Young, EVP of R&D, will stay with the company in a consulting capacity.

Vitestro unveils Aletta robotic phlebotomy device

April 2025—Vitestro unveiled its CE-marked Aletta Autonomous Robotic Phlebotomy Device. Using AI-driven ultrasound guidance, robotic precision, and full automation, Aletta is designed to perform the entire blood draw process, from applying a tourniquet and preparing the skin to vein identification, venipuncture, automated tube handling, and bandage application. The device integrates advanced AI-driven Doppler ultrasound technology to optimize vein selection and needle placement.

ARUP expands AI-augmented screening tool

April 2025—ARUP Laboratories announced the expansion of its AI-augmented screening tool for the detection of human gastrointestinal parasites to include wet-mount slides. The tool uses scanned images to screen and eliminate negative specimens. It aims to reduce ergonomic stressors on laboratory staff, decrease turnaround time, and increase capacity.

Illumina unveils spatial transcriptomics technology

March 2025—Illumina announced a new spatial technology program that the company says will empower researchers to map complex tissues and understand cellular behavior at an unprecedented scale. Enabled on Illumina sequencers and a new multimodal analysis platform, Illumina Connected Multiomics, the spatial technology delivers unbiased whole-transcriptome profiling with cellular resolution and high sensitivity. The technology will allow researchers to examine the spatial proximity of millions of cells per experiment, enabled by a capture area nine times larger than existing technologies and with four times greater resolution. It is compatible with Illumina NextSeq and NovaSeq sequencers.

Leica Biosystems launches HistoCore Chromax WS

March 2025—Leica Biosystems announced the next iteration in its staining and coverslipping portfolio, the HistoCore Chromax Workstation. The HistoCore Chromax WS includes a reagent management system and features graphical, touchscreen interfaces. It is for in vitro diagnostic use and available in select countries.

FDA clears BioFire FilmArray GI Panel Mid

March 2025—BioMérieux announced that its BioFire FilmArray Gastrointestinal (GI) Panel Mid has obtained FDA clearance. The molecular PCR test is capable of simultaneously detecting 11 pathogens directly from a stool sample from individuals presenting with signs or symptoms of gastrointestinal infection. It runs on the BioFire FilmArray 2.0 and Torch PCR platforms, requires about two minutes of hands-on time, and has an approximate run time of one hour. The panel will be commercially available in the United States at the

Court rules in favor of Qiagen in patent dispute

March 2025—Qiagen announced that the German Federal Patent Court has ruled in Qiagen’s favor in a patent dispute against SD Biosensor. The court’s decision upholds Qiagen’s intellectual property rights involving the German part of European patent EP 3 421 997, which protects key innovations in tuberculosis detection. Patents covering these innovations have been issued to Qiagen in several other countries, the company said in a press statement, and form part of a group of more than 120 patents currently issued for QuantiFeron.

Roche unveils sequencing by expansion technology

March 2025—Roche unveiled a proprietary sequencing by expansion (SBX) technology that offers ultra-rapid, high-throughput sequencing that is flexible and scalable for a broad range of applications, including whole genome sequencing, whole exome sequencing, and RNA sequencing. The novel sequencing approach uses a sophisticated biochemical process to encode the sequence of a target nucleic acid molecule (DNA or RNA) into a measurable surrogate polymer called an Xpandomer.

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