Important Milestone for Biotest: Biologics License Application for Fibrinogen Submitted to the US Food and Drug Administration (FDA)
Biotest's Fibrinogen Aims to Fulfill a High Unmet Medical Need for Additional Fibrinogen to Treat Acquired Fibrinogen Deficiency US Submission Follows EU Application for Marketing Authorization ...
Most of the world's 35,000 online pharmacies are run illegally, U.S. warns
Ninety-six percent of online pharmacies were found to violate the law, meaning they were operating without a license and ...
Science Daily19m
Science behind genetic testing for identifying risk of opioid misuse remains unproven
Opioid misuse and specifically opioid use disorder (OUD), continues to represent a significant U.S. public health threat, with more than 6 million Americans aged 12 and older meeting the criteria for ...
JD Supra51m
FDA Updates Final Guidance on Cosmetic Facility Registration and Product Listing: Wiley
The Food and Drug Administration (FDA) recently issued a Notice announcing the availability of an updated final guidance for the industry ...
U.S. FDA sets limits for lead in many baby foods
The U.S. Food and Drug Administration (FDA) this week set maximum levels for lead in baby foods such as jarred fruits and vegetables, yogurts and dry cereal, part of an effort to cut young kids' ...
Hosted on MSN54m
Palforzia’s peanut allergy treatment use in Europe expanded to toddlers
The extension to the marketing authorisation means paediatric patients aged up to 17 years with a confirmed diagnosis of ...
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GAO to FDA: Inspect more domestic, foreign food facilities to ensure safe food supply
On average, the FDA conducted 8,353 routine domestic and 917 foreign food-facility inspections per year from 2018 through ...