Me Vale Madre may be harmful due to hidden drug ingredients
[9-30-2025] The Food and Drug Administration is advising consumers not to purchase or use Me Vale Madre, a product promoted and sold for migraine and stress pain on various websites, including ebay.com, and possibly in some retail stores.FDA laboratory analysis...Natco Pharma Limited – 672564
Delivery Method: Via Email Reference #: 320-24-32 Product: Drugs Recipient: Recipient Name Mr. Rajeev Nannapaneni Recipient Title Vice Chairman and CEO Natco Pharma Limited Natco House Road No: 2, Banjara HillsHyderabad 500034India Issuing Office: Center for Drug...Wholesale Produce Supply of Minneapolis, Minnesota is Recalling Fresh Cut/Processed Cantaloupe, Because it has the Potential to be Contaminated With Listeria Monocytogenes
Summary Company Announcement Date: September 29, 2025 FDA Publish Date: September 29, 2025 Product Type: Food & Beverages Fruit/Fruit Product Foodborne Illness Reason for Announcement: Recall Reason Description Potential to be contaminated with Listeria...Natco Pharma Limited – 672564
Recipient: Recipient Name Mr. Sandeep Kumar Recipient Title Vice President – Quality Natco Pharma Limited Pharma Division, Kothur VillageRangareddy 509228TelanganaIndia Issuing Office: Center for Drug Evaluation and Research (CDER) United States Secondary...CDER Quantitative Medicine Center of Excellence (QM CoE)
The Center for Drug Evaluation and Research (CDER) Quantitative Medicine (QM) Center of Excellence (CoE) is established to facilitate and coordinate the continuous evolution and consistent application of QM for drug development and regulatory decision-making across...Quality and Regulatory Predictability: Shaping USP Standards
On This Page Date: December 11, 2025 Time: 9:00 a.m. – 10:30 a.m. ET Register HereVisit CDER Small Business and Industry Assistance (SBIA) HomepageAbout this Event (Hosted by CDER SBIA)By hosting this workshop, the Association for Accessible Medicines (AAM),...Financial Transparency and Efficiency of PDUFA, BsUFA, and GDUFA
On This Page Date: September 30, 2025 Time: 9:30 a.m. – 10:40 a.m. ET Location: Event Location White Oak Campus: The Great Room FDA Headquarters10903 New Hampshire AvenueBldg. 31, Great Room Conference CenterSilver Spring, MD 20993-0002United States...Early Alerts communicate potentially high-risk removals or corrections
On November 21, 2024, the FDA’s Center for Devices and Radiological Health (CDRH) announced a pilot to minimize the time between the FDA’s initial awareness of a potentially high-risk medical device removal or correction and the agency’s public communication of what...Click To Verify Security & Validation
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