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BioWorld - Monday, January 19, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

March 18, 2020

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Test makers say testing volume ramping up quickly despite concerns over reagents

The U.S. capacity for SARS-CoV-2 testing is limited by several items, including the swabs used to collect patient specimens, but the supply of reagents has been front and center recently. Despite those concerns, several private test makers said they are quickly ramping up production, including Thermo Fisher Scientific Inc., of Waltham, Mass., which said it has enough supplies of all types on hand to provide 2 million reactions per week, a volume that should increase to 5 million per week in April. Read More
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White House: Much more money needed to battle COVID-19

As the world goes to war with COVID-19, the U.S. is ripping open the purse strings to fund mobilization against both the coronavirus and the economic devastation it’s causing. Read More
Ocular-eye

Eye disease-focused Sight Sciences raises $30M in series E

Sight Sciences Inc., of Menlo Park, Calif., scooped up $30 million in a series E preferred stock financing round that was led by D1 Capital Partners. The funds are earmarked to further advance clinical and operational development and support commercial expansion of the company’s Omni surgical and Tearcare systems. Read More
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Ventec joins COVID-19 fight with multifunction ventilator

With the high need for ventilators in the face of COVID-19, Ventec Life Systems, of Bothell, Wash., is stepping up with its multifunction ventilator, known as VOCSN, for ventilation, oxygen, cough, suction and nebulization. Read More
coronavirus covid-19 headlines

Verily uses COVID-19 to expand Project Baseline, aims to quell rampant privacy concerns

Google sister company Verily Life Sciences LLC has been under an unprecedented amount of scrutiny since it was promoted over the weekend by President Donald Trump as responsible for a nationwide information and testing program for the emerging novel coronavirus. Read More
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TGA refines proposals to reclassify six groups of medical devices based on industry comments

PERTH, Australia – Six classes of medical devices listed on Australia’s Register of Therapeutic Goods (ARTG) will fall under new classification requirements on Aug. 25, 2020, following numerous consultations with industry. The consultations were part of the Australian government’s plans to overhaul its medical device regulations to be more in line with the European Medical Device Regulation (MDR). Read More

Appointments and advancements for March 18, 2020

New hires and promotions in the med-tech industry, including: Endologix. Read More

Financings for March 18, 2020

Med-tech firms raising money in public or private financings, including: E25bio, Helius Medical Technologies, Venus Concept. Read More

Other news to note for March 18, 2020

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Ambu, ATTC, Biointellisense, Biomerica, Bio-Techne, Centogene, Clinical Laserthermia Systems, Dover, Em-tec, Llamasoft, MeMD, Myriad Genetics, Oxford Nanopore Technologies, Pacific Biosciences of California, Parallax Health Sciences, Qiagen, Rewalk Robotics, Startx, Tomi Environmental Solutions, Tabula Rasa Healthcare, Windgo. Read More

Regulatory actions for March 18, 2020

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Canon Medical, Quidel. Read More

Regulatory front for March 18, 2020

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

BioWorld MedTech’s Orthopedics Extra for March 18, 2020

Keeping you up to date on recent developments in orthopedics, including: Vitamin D boosts chances of walking after hip fracture; Rsip Vision reports breakthrough AI tech for 3D reconstruction of knees; Study shows disparities in outpatient care for common orthopedic problems. Read More

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