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- FDA approves Firazyr to treat acute attacks of hereditary angioedema
- FDA working with Mexico to protect safety of imported papayas
- FDA hurricane preparedness checklist
- FDA approves Xalkori with companion diagnostic for a type of late-stage lung cancer
- FDA: U.S. Marshals seize food products held at North Carolina warehouse
- FDA Commissioner Margaret A. Hamburg’s Statement on the Passing of Dr. Charles Edward
- FDA announces new staff training for medical device reviewers
- FDA: Pilot projects to explore ways to trace sources of foodborne illness
- FDA warns consumers of botulism risk in La Ruche tapenade, spreadable tomato paste
- FDA announces changes in drug center’s oncology office
- FDA investigates multistate outbreak of listeriosis
- FDA: Minnesota companies agree to halt sale of amino-acid products with unapproved c
- FDA establishes foodborne illness outbreak response network
- FDA warns consumers not to eat Rocky Ford Cantaloupes shipped by Jensen Farms
- FDA confirms Listeria monocytogenes on Jensen Farms? Rocky Ford-brand cantaloupes
- FDA: Over-the-counter asthma inhalers containing chloroflouorocarbons (CFCs) will no
- FDA approves Soliris for rare pediatric blood disorder
- FDA approves Remicade to treat ulcerative colitis in children older than 6 years
- FDA Warns Consumers Not to Eat Raw Oysters Harvested from Hood Canal Area 4 in Washin
- FDA clears first single use face mask for children
- FDA enters consent decree of permanent injunction against Florida drug companies
- FDA participates in global efforts to protect consumers and patients from unsafe drug
- FDA seeks comment on streamlined review of lower risk, new technology, devices
- FDA: New transparency report outlines proposals for enforcement data, for public comm
- FDA works to improve science used to approve medical devices
- FDA awards three grants to stimulate development of pediatric medical devices
- FDA Outlines Plans for an Outside Network of Scientific Experts
- FDA approves gel to stop blood flow during blood vessel surgery
- FDA commissioner outlines steps to spur biomedical innovation, improve health of Amer
- FDA and NIH announce joint study on tobacco use and risk perceptions
- FDA approves Cialis to treat benign prostatic hyperplasia
- FDA approves combination therapy Juvisync
- FDA, CMS launch pilot program for voluntary parallel review of innovative devices
- FDA: U.S. Marshals seize foods stored at Washington State facility
- FDA approves Ferriprox to treat patients with excess iron in the body
- FDA proposes lower risk classification, special controls for external pacemakers
- FDA: U.S. Marshals seize food products at Illinois warehouse
- FDA approves Onfi to treat severe type of seizures
- FDA approves first generic olanzapine to treat schizophrenia, bipolar disorder
- FDA invests $2 million in partnerships through Centers of Excellence in Regulatory Sc
- FDA warns consumers not to eat Wegmans’ bulk Turkish pine nuts
- FDA Enters Consent Decree of Permanent Injunction in NY Tissue Residue Case
- FDA approves system to repair abdominal aneurysms in people with small arteries
- The U.S. Food and Drug Administration today approved the first artificial heart valve
- FDA: 35 innovative new drugs approved in fiscal year 2011
- FDA approves Xarelto to prevent stroke in people with common type of abnormal heart r
- FDA warns consumers not to eat Bio Gaudiano brand Organic Olives Stuffed with Almonds
- FDA warns consumers not to eat certain ASSI Brand frozen oysters
- FDA approves Erbitux to treat late-stage head and neck cancer
- FDA launches website on safe disposal of used needles and other “sharps”
- FDA Statement on Makena
- FDA acts to protect children from illegal tobacco sales
- FDA approves first cord blood product
- FDA issues two draft guidance documents to facilitate investigational medical device
- FDA approves first drug to treat a rare bone marrow disease
- FDA Statement on the International Tobacco Regulators' Conference
- FDA approves Erwinaze to treat a form of leukemia
- FDA Commissioner announces Avastin decision
- FDA approves first supplemental test for Chagas disease
- FDA approves Eylea for eye disorder in older people
- FDA warns consumers not to eat one batch of Loyd Grossman Korma Sauce
- FDA permits marketing of a system to repair failed, problematic fix for aortic aneury
- FDA takes enforcement action against Pennsylvania dietary supplement maker
- FDA approves first insomnia drug for middle-of-the-night waking followed by difficult
- FDA approves first generic version of cholesterol-lowering drug Lipitor
- FDA outlines flexible approaches for artificial pancreas system clinical trials, prod
- FDA: U.S. Marshals seize dietary supplements, drugs manufactured by Syntec Inc.
- FDA, FTC act to remove “homeopathic” HCG weight loss products from the market
- FDA: U.S. Marshals seize products containing banned ephedrine for dietary supplements
- FDA announces changes to risk strategy requirements for 2 drugs to treat low platelet
- FDA issues Warning Letters for misleading advertising of Lap-Band
- FDA permits marketing of the first hand-held device to aid in the detection of bleedi
- FDA Statement on the Institute of Medicine Report: Scientific Standards for Studies o
- FDA proposes draft guidelines intended to improve the representation of women in medi
- FDA approves mechanical cardiac assist device for children with heart failure
- FDA collaboration to monitor rare eye condition associated with cataract surgery
- FDA expands use of HIV drug Isentress to children and adolescents
- FDA: Do not use ShoulderFlex Massager
- FDA: Chicago-area sandwich manufacturer agrees to stop production
- FDA to approve shared system REMS for TIRF products
- FDA expands use of Prevnar 13 vaccine for people ages 50 and older
- FDA to protect important class of antimicrobial drugs for treating human illness
- FDA completes work on three drug user fee programs
- FDA expands use of endovascular graft to treat aortic tears
- FDA approves Voraxaze to treat patients with toxic methotrexate levels
- FDA permits marketing of first test for risk of rare brain infection in some people t
- Maine company holds cold smoked salmon product after FDA order
- Department of Justice files Consent Decree of Permanent injunction against Ranbaxy
- FDA approves Inlyta to treat patients with a type of advanced kidney cancer
- FDA approves new treatment for most common type of skin cancer
- FDA takes action against New York cheese manufacturer
- FDA approves Kalydeco to treat rare form of cystic fibrosis
- FDA approves Gleevec for expanded use in patients with rare gastrointestinal cancer
- FDA and industry reach agreement in principle on medical device user fees
- FDA issues draft guidance on biosimilar product development
- FDA investigating illegal online sale of handheld dental X-ray units
- New Jersey company agrees to halt production of unapproved dental devices
- FDA seeks $4.5 billion to support medical product development, protect patients and e
- FDA approves Zioptan to treat elevated eye pressure
- FDA approves Korlym for patients with endogenous Cushing’s syndrome
- FDA acts to bolster supply of critically needed cancer drugs
- Federal government gains permanent injunction against raw milk producer
- FDA approves first Helicobacter pylori breath test for children
- FDA reaches $1 million settlement with Pennsylvania medical device firm
- FDA announces safety changes in labeling for some cholesterol-lowering drugs
- FDA approves first quadrivalent vaccine to prevent seasonal influenza
- FDA approves two new pancreatic enzyme products to aid food digestion
- La FDA anuncia modificaciones relacionadas con la seguridad en las indicaciones de al
- FDA issues warning letter to makers of AeroShot ?caffeine inhaler?
- FDA approves Surfaxin to prevent breathing disorder in premature infants
- FDA Commissioner Margaret A. Hamburg's Statement on the Surgeon General's Report
- La FDA aprueba nuevos implantes de seno rellenos de gel de silicona
- FDA approves new silicone gel-filled breast implant
- FDA approves first cell-based product to treat oral mucogingival conditions in adults
- FDA approves first generic Lexapro to treat depression and anxiety disorder
- FDA proposes lower risk classification for certain tuberculosis tests
- FDA approves first Boniva generics to treat or prevent osteoporosis
- FDA approves LINX Reflux Management System to treat gastroesophageal reflux disease
- FDA approves Omontys to treat anemia in adult patients on dialysis
- New FDA guidance on considerations used in device approval, de novo decisions
- FDA approves additional blood test for viruses linked to leukemia, neurologic disease
- FDA to discuss risks and benefits of metal-on-metal hip replacements
- FDA pursues enforcement action against California fish processor
- U.S. Marshals seize unapproved and misbranded drug products at Missouri distributor
- Obama administration takes action to address tobacco epidemic
- FDA warns consumers not to eat Crispy brand cookies and rusk manufactured by TWI Food
- FDA enters consent decree with cheese producer due to Listeria contamination
- FDA announces plans to pilot end-stage kidney disease technology in new program
- FDA approves imaging drug Amyvid
- FDA takes steps to protect public health
- Dept. of Justice enters consent decree with California seafood processor
- Moon Marine USA Corporation voluntarily recalls frozen raw yellowfin tuna product
- U.S. Marshals seize ultrasound gel product at a New Jersey company
- FDA issues draft guidance on nanotechnology
- Report: FDA strengthens monitoring of post-approval drug safety
- FDA strengthens international collaboration to ensure quality, safety of imported pro
- FDA Statement on USDA Announcement of Positive BSE Test Result
- FDA approves Afinitor for non-cancerous kidney tumors caused by rare genetic disease
- FDA approves Votrient for advanced soft tissue sarcoma
- FDA approves Stendra for erectile dysfunction
- FDA challenges marketing of DMAA products for lack of safety evidence
- FDA approves new antibacterial treatment for plague
- FDA approves new orphan drug to treat a form of Gaucher disease
- FDA permits marketing of a new device for abdominal surgery
- FDA issues final rule on sterility testing of biological products
- FDA proposal aims to help reduce unnecessary radiation exposure for children
- FDA issues alert on potential dangers of unproven treatment for multiple sclerosis
- FDA expands use for FilmArray Respiratory Panel
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