by Bruce Waldon | Dec 11, 2025 | Consumer Information, Dietary Supplements, DSHEA, Editorial, FDA_Legislation, Industry Information, Industry News, Legislation, Product Quality
DSHEA Reform Why it must be a priority Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Why DSHEA Reform Must Be a Priority The recent wave of moringa-related...
by Bruce Waldon | Dec 11, 2025 | Alerts, Alerts-Supplements, Consumer Information, Dietary Supplements, DSHEA, Industry Information, Industry News, Legislation, MedWatch-System, Product Quality, Quality Information, Safety
The 30-Year Consequences of DSHEA A direct cause of the supplement safety crisis Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact How a 1994 Law Created Today’s...
by Bruce Waldon | Dec 11, 2025 | Alerts, Alerts-Supplements, Consumer Information, Consumer Safety, Dietary Supplements, DSHEA, Editorial, FDA Regulations, FDA_Legislation, Industry Information, Industry News, Legislation, Product Quality, Product Recalls, Quality Information, Reg_Information, Reg_Products, Regulatory_Info, US-FDA
The Invisible Outbreak An untraced distribution of salmonella-contaminated products Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact Contaminated Products...
by Bruce Waldon | Nov 14, 2025 | Alerts, Alerts-Supplements, Consumer Information, Consumer Safety, Dietary Supplements, FDA Public Information, FDA Regulations, Industry Information, Industry News, Product Quality, Product Recalls, Product Safety, Regulatory_Info, US-FDA
Recall Alert: Organic Moringa Leaf Powder The product may be contaminated with salmonella bacterium Home About Consumer Regulatory Medical Devices Pharma Biologics Combination Products AI Quality QMSR Central News Enforcement Alerts Innovation Contact On November 12,...
by MDP Staff | Aug 7, 2025 | FDA Public Information, FDA_Innovation, Industry Information, Industry News, New Pharma Products, Pharmaceuticals
“PreCheck” Program to Boost U.S. Drug Manufacturing Program supports facilities certification and drug submissions Home About Consumer Medical Devices Medical Device Warning Letters Pharma Pharma Warning Letters Biologics Biologics Warning Letters AI Regulatory...
by MDP Staff | Jul 24, 2025 | EU MDR, FDA Reports, Global-RA, Industry Information, MDR - Medical Device Report, Med-Devices, US-FDA
Global Medical Device Reporting and Vigilance Reporting serious safety risks Home About Consumer Medical Devices Pharma AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact International Medical Device Reporting Medical Device Reporting and...
