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BioWorld - Wednesday, February 4, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Oct. 29, 2019

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Genomics-focused Pieriandx closes $27M series B

St. Louis-based Pieriandx, a clinical genomics informatics company, reported that it has closed a $27 million series B funding round led by Atw Partners and Sjf Ventures. Pieriandx provides a software-as-a-service platform that the company says permits the practice of clinical genomics as a standard of care. Read More

Veracyte touts early results in nasal swab test for early lung cancer detection, revenue up to $31M

Genomic testing firm Veracyte Inc. is eyeing 2021 for the launch of its noninvasive nasal swab classifier for early lung cancer detection and diagnosis, following preliminary clinical data demonstrating high sensitivity in low-risk patients and high specificity in high-risk patients with known lung nodules. The South San Francisco-based company is developing the nasal swab test in collaboration with Johnson & Johnson Inc.'s Lung Cancer Initiative, part of a long-term strategic collaboration that also aims to speed commercialization of Veracyte's Percepta genomic sequencing classifier. Read More

Pfizer tracking lung cancer resistance profile using Inivata's liquid biopsy tool

LONDON – Pfizer Inc. is taking further steps to distinguish its third-generation anaplastic lymphoma kinase (ALK) inhibitor, Lorbrena, from the rest of the field, funding a pan-European trial that will use liquid biopsies to track the resistance profile of non-small-cell lung cancers (NSCLC). Read More

Role of manufacturer labs emphasized in ASCA pilot program

The FDA held a webinar directed toward the recent draft guidance for the accreditation scheme for conformity assessment (ASCA), but while independent labs figure to handle much of the related activity, FDA staff welcomed manufacturer's labs as well, emphasizing that the agency seeks the participation of all potentially interested parties. Read More
Patient receiving dialysis

Fresenius gets breakthrough designation for hemodialysis system to prevent blood clots

The U.S. FDA has granted a breakthrough device designation for a new hemodialysis system from Fresenius Medical Care Holdings Inc. The device is designed to prevent blood blotting without the use of blood-thinning medication, such as heparin, that most dialysis patients require. Read More

Other news to note

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief. Read More

Appointments and advancements

New hires and promotions in the med-tech industry. Read More

Daily M&A

Mergers and acquisitions in the med-tech industry. Read More

Financings

Med-tech firms raising money in public or private financings. Read More

Regulatory front

The latest global regulatory news, changes and updates affecting medical devices and technologies. Read More

Product clinical data for Oct. 28, 2019

Clinical updates, including trial initiations, enrollment status and data readouts and publications. Read More

BioWorld MedTech's Cardiology Extra

Keeping you up to date on recent developments in cardiology. Read More

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