Truveta Data expands beyond EHR data with linked closed claims for more than 200 million patients
Truveta delivers the most representative, complete, and timely patient journey data, exceeding FDA standards of data quality, data provenance, and audit readiness. With EHR data from more than 120 ...
UFC, Thorne renew global partnership
Holdings, and Thorne, a company in science-backed health and wellness solutions, announced a renewal of their global partnership, featuring enhancements that will strengthen the collaboration. Under ...
BGR15d
FDA approved the first new kind of pain medication in 27 years. Here’s how it works
If you buy through a BGR link, we may earn an affiliate commission, helping support our expert product labs. For the first time in over two decades, the U.S. Food and Drug Administration (FDA) has ...
Today15d
FDA approves new type of nonopioid painkiller for acute pain
The Food and Drug Administration on Thursday approved a new type of nonopioid painkiller from Vertex Pharmaceuticals. The drug, Journavx, or suzetrigine, was approved to treat moderate to severe ...
News Medical15d
New FDA initiatives focus on medication safety for pregnant and nursing women
When the U.S. Food and Drug Administration approves a prescription medication for adults, the drug is also approved for pregnant patients. But information about medication dosing during pregnancy ...
Today17d
Lay’s potato chip recall elevated to FDA’s highest-risk classification
The Food and Drug Administration just raised its recall of Lay’s Classic Potato Chips to the highest risk level. On Dec. 16, Frito-Lay issued a recall for 6,344 (13-ounce) bags of Lay’s ...
The Bakersfield Californian19d
Medimaps Breaks New Ground in Fracture Risk Assessment with FDA Clearance and MDR Certification for TBS Osteo Next Generation Software
medimaps group S.A., a global leader in AI-driven bone microarchitecture imaging solutions, proudly announces 510(k) clearance from FDA and MDR certification in EU for the latest version of its ...
Yahoo Finance19d
Medimaps Breaks New Ground in Fracture Risk Assessment with FDA Clearance and MDR Certification for TBS Osteo Next Generation Software
GENEVA, January 27, 2025--(BUSINESS WIRE)--medimaps group S.A., a global leader in AI-driven bone microarchitecture imaging solutions, proudly announces 510(k) clearance from FDA and MDR certification ...
Business Wire22d
Global Drug Safety & Pharmacovigilance Regulatory Requirements and Certification Training Course with Focus on EU and US (ONLINE EVENT: February 12, 2025 / ON-DEMAND ...
DUBLIN--(BUSINESS WIRE)--The "Global Regulatory Requirements for Drug Safety & Pharmacovigilance Certification Program" training has been added to ResearchAndMarkets.com's offering. This training ...
NBC News24d
Federal regulations paused, halting FDA's proposed ban on formaldehyde in hair products
The Food and Drug Administration announced it would decide by April 2024 whether chemical hair straightening products sold in the U.S. would be banned from using formaldehyde or ingredients that ...
Newsweek24d
FDA Approves Nasal Spray for Depression
and misuse," the drug will only be available through a restricted program through certified treatment centers. What People Are Saying Bill Martin, Ph.D., Global Therapeutic Area Head, Neuroscience ...