Elon Musk’s Neuralink says it has FDA approval for study of brain implants in humans
Elon Musk’s Neuralink says it has FDA approval for study of brain implants in humans May 25 (Reuters) – Elon Musk’s brain-implant company
Elon Musk’s Neuralink says it has FDA approval for study of brain implants in humans May 25 (Reuters) – Elon Musk’s brain-implant company
Krystal gets first FDA approval for redosable gene therapy, rare skin disease Published: May 22, 2023 By Tristan Manalac BioSpace The FDA
Lawsuits endanger FDA role on approvals By Jon Bigelow While media attention has focused on the availability of abortions, take note: contradictory
The use of artificial intelligence (AI) in healthcare has been growing rapidly in recent years, and AI-enabled medical devices are playing a
Republicans are in a weird state of flux and mostly can't agree on a cohesive message. Can we say "Republicans in disarray!" or
Late last night, three-judge panel for the Fifth Circuit stayed (partially) the decision last week from Judge Matthew J. Kacsmaryk, which ruled that
NICE Backs PTC’s gene therapy for ultra-rare pediatric disease Published: Mar 24, 2023 By Tristan Manalac BioSpace England’s National Institute
Back in the spine-tingling hysteria of the dotcom boom in the late 1990’s, when investors threw dump trucks of money at dotcom startups, I sat with
When I last came to SXSW, Austin’s high rent version of Mardi Gras, in the ancient mid 90s, it was all about the bands. Times change. This year, as
Company plans to initiate phase I/IIa in-human clinical trials in Q2 2023 Tel Aviv, Israel / Vancouver, Canada, March 16, 2023 (GLOBE NEWSWIRE)
Neuralink, other brain-chip makers face long road to FDA approval By Marisa Taylor March 2 (Reuters) – Neuralink, founded in 2016, has yet to
In continuation of my update on LatanoprostThea Pharma, Inc. (“Thea”), the U.S. subsidiary of Europe’s leading independent pharmaceutical
Rigel Pharmaceuticals, Inc. announced the U.S. Food and Drug Administration (FDA) approval of Rezlidhia (olutasidenib) capsules for the
Mirati Therapeutics, Inc. (NASDAQ: MRTX), a targeted oncology company, announced the U.S. Food and Drug Administration (FDA) approval
In continuation of my update on Phenyl butyrate Acer Therapeutics Inc. and its collaboration partner, RELIEF THERAPEUTICS Holding SA