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BioWorld - Monday, May 18, 2026
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Medical technology
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Financings for March 16, 2021

March 16, 2021
Med-tech firms raising money in public or private financings, including: Clarify Health, Glooko, Nephrosant, Revelation Partners.
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Appointments and advancements for March 16, 2021

March 16, 2021
New hires and promotions in the med-tech industry, including: Izotropic, Navaderm Partners, Ontrak.
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BioWorld MedTech’s Oncology Extra for March 16, 2021

March 16, 2021
By Mark McCarty and Anette Breindl
Keeping you up to date on recent developments in oncology, including: Rethinking dose fractionation in radiotherapy for prostate cancer; Immune system, treatment, in kidney cancer; Targeting membrane protein starves pancreatic tumors; Olive oil, not just for pasta anymore.
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Chess board and pieces, blocks spelling out M&A

New working group to take deep dive on biopharma M&As

March 16, 2021
By Mari Serebrov
A new multilateral working group could bring deeper scrutiny to biopharma mergers, both past and future. The group, made up of competition experts from Canada, the EU, U.K. and U.S., is taking on the job of identifying fresh approaches to analyze and address the competitive concerns raised by biopharma M&As.
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Hands holding arrow-shaped puzzle pieces

Roche acquiring Genmark in $1.8B merger

March 15, 2021
By Annette Boyle
Roche Holding AG will acquire Genmark Diagnostics Inc. for $24.05 per share in cash for a total of $1.8 billion on a fully diluted basis. The transaction will give Basel, Switzerland-based Roche access to Genmark’s molecular diagnostics portfolio. The deal is expected to close in the second quarter of 2021. The price represents a 43% premium on the Carlsbad, Calif.-headquartered diagnostics company’s share price as of Feb. 10, prior to media speculation about a potential acquisition.
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Medicare puzzle

CMS suspends implementation date for breakthrough devices coverage policy

March 15, 2021
By Mark McCarty
The U.S. Centers for Medicare & Medicaid Services (CMS) has imposed a 60-day delay in the implementation of the Medicare Coverage of Innovative Technologies (MCIT) program, stating that the MCIT draft rule was developed under a flawed assumption about the volume of eligible breakthrough devices. CMS said the situation suggests that the public did not have an appropriate opportunity to comment on the proposed rule, a predicament that suggests the possibility that the MCIT program might not survive the Biden administration’s regulatory review.
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DNA, dollars illustration

Variantyx scoops up $20M for whole genome sequencing-based testing methodology

March 15, 2021
By Meg Bryant
Variantyx Inc. raised $20 million in a series C financing led by GHS Fund (Quark Venture LP and GF Securities). The new funds are earmarked for the development of comprehensive tumor diagnostic solutions and sales expansion. Also taking part in the round were new investor IBM Ventures and existing investors Pitango Venture Capital, New Era Capital Partners and 20/20 Healthcare Partners. With this latest infusion, Variantyx has raised a total of $38 million.
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Datar wins CE mark for Trublood cancer detection system

March 15, 2021
By Nuala Moran
LONDON – Following circulating tumor cells and cell-free tumor DNA, a new type of liquid biopsy is poised for commercial rollout after Datar Cancer Genetics Ltd. secured CE marking for Trublood, a method for isolating tumor cell clusters. In fact, the clusters do not consist solely of tumor cells, but can also include endothelial cells, erythrocytes, stromal cells, leukocytes, platelets, and cancer-associated fibroblasts. They are held together by cell-to cell-adhesion proteins.
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Person holds artificial heart in hands

Carmat raises $66.4M to launch its artificial heart in Europe

March 15, 2021
By Bernard Banga
PARIS – Carmat SA has just completed a capital increase of $66.4 million to boost development of its total artificial heart. The Aeson system was awarded CE marking four months ago, as a total bridge to transplantation for patients suffering with end-stage biventricular heart failure who are not eligible for maximal medical therapy or a left ventricular assist device (LVAD), and who are likely to undergo a heart transplant within 180 days of the implantation.
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Regulatory front for March 15, 2021

March 15, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA comments on two patent term extensions; Comment period reopened on Orange Book patents.
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