Fda Press Releases

Daryl Guberman, a 40-year quality assurance expert, exposes the deep-rooted corruption within laboratory accreditation bodies like ANSI-ANAB and A2LA, which have facilitated widespread fraud and regulatory failures.

Exposing Boeing, The American National Standards Institute (ANSI), The American National Accreditation Board (ANAB), and Federal Agencies in a Supplier Audit Cover-Up—A Web of Corruption and Regulatory Failure.

Federal Agencies, Corporations, and Private Accreditation Bodies: How Fauci, NIH, CDC, Pfizer, Johnson & Johnson, and Government Officials Are Entangled in Ethical and Legal Violations.

"40+ Year QA Expert Daryl Guberman Exposes Global Accreditation Failures": How Conflicts of Interest and Regulatory Lapses Endanger Lives in Aerospace, Medical, Automotive, and Electronics Industries—Wake Up Before the Next Catastrophe"

AATCLC Holds News Conference/Rally Thursday, January 16, 2025 in Oakland Protesting FDA Attempt to Dismiss Lawsuit to Ban Menthol From Cigarettes That Would Save Black Lives.

"COVID Vaccine Makers Shielded from Liability Until 2029: QA Expert Daryl Guberman Reveals Path for Injured Individuals to Seek Justice and Exposes Systemic Quality Failures"

Actuated Medical, a leading innovator in medical device technologies, proudly announces the receipt of a second FDA 510(k) clearance for its GripTract-GI™ Endoscopic Tissue Manipulator (GripTract) product line.

Daryl Guberman, a veteran quality management expert with over four decades of experience, has revealed a troubling gap in Boeing's supplier oversight practices.

Please+Publish is specifically designed to empower small businesses saving time and costs in regulatory publishing.

Nova Biomedical announces the U.S. launch of our New Generation StatStrip Glucose Hospital Meter System.

Actuated Medical, a leading innovator in medical device technologies, proudly announces the receipt of FDA 510(k) clearance for its groundbreaking GripTract-GI™ Endoscopic Tissue Manipulator (GripTract-GI).

Hoth Intelligence, a health care augmented reality software company, announced today that the U.S.

SHF 2.0 Framework as Practical Solution to Drive Continuous Improvement

Devices not cleared by the FDA are being sold in the USA! Buying non-FDA cleared devices can cause injury. Spa Sciences launches LEXI after receiving FDA clearance for effective treatment.