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Lantheus Holdings has secured the US Food and Drug Administration (FDA) supplemental new drug application (sNDA) approval for VIALMIXRFID device, for use with DEFINITY Vial. The medical equipment
Sherlock Biosciences has entered into a research collaboration with Dartmouth-Hitchcock Health (D-HH) to begin clinical trial of its Sherlock CRISPR SARS-CoV-2 kit for the detection of Covid-19-causing coroanvirus.
Quidel Corporation (NASDAQ: QDEL) (“Quidel”), a provider of rapid diagnostic testing solutions, cellular-based virology assays and molecular diagnostic systems, announced today that Quidel has received Health Canada authorization
IDEXX Laboratories, Inc. (NASDAQ: IDXX), a global leader in veterinary diagnostics and software, announced today the launch of the ProCyte One™ Hematology Analyzer. The new analyzer’s advanced technology
US-based Hologic has validated its Aptima and Panther Fusion assays for molecular diagnosis of Covid-19 using pooled patient samples. The company has also filed an emergency use notification
Deep Blue Medical Advances has obtained the US Food and Drug Administration (FDA) 510(k) approval for its T-Line Hernia Mesh with integrated suture-like extensions. The surgical instruments maker
FDA has cleared MagVenture TMS Therapy® for adjunct treatment of Obsessive-Compulsive Disorder (OCD). This marks the second indication in the US for the Danish medical device company MagVenture
The Wyss Center for Bio and Neuroengineering has granted a worldwide license to Blackrock Microsystems to commercialize its neural signal processing and decoding software platform for research and
Thermo Fisher Scientific has developed a new serological assay, dubbed LABScreen COVID Plus Assay, to help transplant candidates and recipients by detecting antibodies against Covid-19. The company’s transplant
Israeli startup PulseNmore today announced the launch of its flagship handheld tele-ultrasound device that enables pregnant women to perform at-home ultrasound scans, and receive feedback from a physician