BioSpace News Archive

Porokeratosis is a rare skin disorder which may develop skin cancer in adverse case resulting from abnormal clonal expansion of keratinocytes.

The growing influence of technology across the life science research, molecular diagnostics, and forensics will boost the growth of the nucleic acid isolation and purification market through the assessment period of 2020-2030.

Ascentage Pharma (6855.HK), a globally focused, clinical-stage biotechnology company engaged in developing novel therapies for cancers, chronic hepatitis B (CHB), and age-related diseases, today announced its appointment of Dr. David Sidransky , MD.

VERO Biotech LLC, an Atlanta, Georgia -based biotechnology company focused on saving lives, alleviating suffering, and improving the health economics of care, today announced that the company was awarded the coveted Golden Helix “Best Deal of the Year” Award for 2021 by Georgia Bio, the state’s life science trade association. VERO Biotech was recognized in the category of Private Financing, in a virtual awards ceremony last night.

S4 Medical moves a step closer in developing the most comprehensive solution to protect the esophagus from thermal injury during catheter ablation procedures for atrial fibrillation (AF) with the closing of their Series A financing.

With COVID-19 vaccines now available for millions and eligibility soon open to everyone, Americans are eager to get back to what matters most.

Fuse Medical, Inc. (OTCPINK: FZMD) (“Fuse” or the “Company”) an emerging manufacturer and distributor of innovative medical devices for the orthopedic and spine marketplace, announced that it has filed its annual report on Form 10-K for the year ended December 31, 2020 with the Securities and Exchange Commission (“SEC”) on Tuesday, March 30, 2021.

Pfizer Inc. (NYSE: PFE) invites investors and the general public to access a live video webcast of a presentation and conference call with investment analysts at 10 a.m. EDT on Friday, April 9, 2021.

NANO-X IMAGING LTD (NASDAQ: NNOX) (“Nanox” or the “Company”), an innovative medical imaging technology company, announced today that its single-source Nanox.ARC digital x-ray technology has received 510(k) clearance from the US Food and Drug Administration (the “FDA”).

eMed™, the architect behind the first BinaxNOW™ at-home COVID-19 test kit, announces the non-prescription home use availability of third-party guided and verified COVID-19 at-home tests for asymptomatic serial testing and screening, with results accepted by many airlines and businesses using the Abbott BinaxNOW™ home test and eMed telehealth services.