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, 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 Bruce Waldon | Nov 6, 2025 | Design and Development, Design Changes, FDA Regulations, Human Factors, Industry News, International standards, ISO 13485, ISO 14971, Med-Devices, Product Design, Product Quality, QMSR, Safety, US-FDA
When a “Good Enough” Design May Fail the User A Case Study in Usability Home Request Info QMSR Central QMSR FAQs ISO 13485 Transition Impact Integration Definitions FDA and ISO 13485 ISO 9000 Small Manufacturers Advancing from Basic Design to Usability In a world...
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 25, 2025 | Alerts, Alerts-Device, Class I Recalls, FDA Safety Communication, Industry News, Med-Devices, Product Recalls, Product Safety, Safety, Surgical
Ethicon Issues Safety Alert for Endopath Echelon Vascular Reload Surgical Stapler Cartridge Correction Home About Consumer Medical Devices Pharma Biologics Biologics Warning Letters AI Regulatory Quality QMSR Central News Enforcement Alerts Innovation Contact Endopath...
