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"FDA is badly broken" - Senior Congress Members
Congress has criticized the Food and Drug Administration (FDA) in the past year for not ensuring the safety of the nation's food, prescription drug an...

FDA Warns Consumers Not to Use “Blue Steel” and “Hero” Products
The U.S. Food and Drug Administration is advising consumers not to purchase or use "Blue Steel" or "Hero" products marketed as dietary supplements thr...

Ingenuity Systems Delivers Key Milestones in FDA Collaboration to Facilitate Genomic Data Review
Ingenuity Systems, provider of information solutions for life science researchers, announced it has achieved key milestones in the ongoing Cooperative...

FDA Discusses Challenges of Global Food Supply on Final Day of the 10th Annual Food Safety & Securit
FDA and State Interactions: Addressing Changes and Challenges for Food Supply Safety will be discussed during the final keynote presentation at the 10...

FDA Approves New Medical Adhesive to Treat Burn Patients
The U.S. Food and Drug Administration today approved a new medical adhesive (a fibrin sealant) called Artiss for use in attaching skin grafts onto bur...

FDA Warns of Salmonella Risk with Cantaloupes from Agropecuaria Montelibano
The U.S. Food and Drug Administration has issued an import alert regarding entry of cantaloupe from Agropecuaria Montelibano, a Honduran grower and pa...

Global Research Services and CardioDynamics Global Research Services Sign Strategic Alliance Agreement
Global Research Services, LLC (GRS) entered into a strategic alliance with CardioDynamics. The agreement authorizes GRS to utilize CardioDynamics’ imp...

FDA Indicates That Genasense Approval in Chronic Lymphocytic Leukemia Will Require Additional Confirmatory Data
Genta Incorporated announced that the Food and Drug Administration's (FDA) Center for Drug Evaluation and Research (CDER) has decided that available d...

Duska Therapeutics Plans Meeting with the FDA on ATPace
Duska Therapeutics, a biotechnology company developing medical products based on adenosine 5'-triphosphate (ATP) and P2 receptor-related technologies,...

FDA Approves Nexium for Use in Children Ages 1-11 Years
The U.S. Food and Drug Administration approved Nexium (esomeprazole magnesium) for short-term use in children ages 1-11 years for the treatment of gas...

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