They hoped the board would establish rules that would foster the fledgling adult stem-cell therapy -- which is not FDA-approved and has so far had mixed evidence of success -- not hinder it. The board took another approach. In draft rules floated in Augu
• Pharma News
Powered By DaylifeOther company news pages:
- Abbott Labs
- Amgen
- AstraZeneca
- Bristol-Myers Squibb
- Eli Lilly
- Glaxo
- Roche
- J&J
- Merck
- Novartis
- Pfizer
- Sanofi-Aventis
- Schering-Plough
- Wyeth
Food and Drug Administration News
Release of FDA Guidance for Biosimilars Pathway Marks Important Step Forward, Says BIO
WASHINGTON--(BUSINESS WIRE)-- Biotechnology Industry Organization (BIO) President and CEO Jim Greenwood issued the following statement regarding the newly released U.S. Food and Drug Administration (FDA) guidance for the review and approval of biosimilar
Mylan Doxycycline Hyclate tablets win FDA ANDA approval
Nanotechnology in Drug Delivery - Technological Improvements and Novel Approaches to Fulfill High Potential GBI Research, the leading business intelligence provider, has released its latest report, “Nanotechnology in Drug Delivery - Technological Improve
Fear Causes Backlash Against OJ After Fungicide Found in Imports
LAKELAND | Florida citrus may be realizing one of its worst fears — a consumer backlash against purchasing orange juice out of fear of contamination by the banned fungicide carbendazim. Meanwhile, the U.S. Food and Drug Administration reported Thursday i
Mylan's generic Doryx ANDA receives final FDA approval
Mylan Inc. (Nasdaq: MYL) today announced that its subsidiary Mylan Pharmaceuticals Inc. has received final approval from the U.S. Food and Drug Administration (FDA) for its Abbreviated New Drug Application (ANDA) for Doxycycline Hyclate Delayed-release (
Wholistic Herbs, Inc. Recalls "Koff & Kold" and "Kold Sore" Because Of Possible Health Risk
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. FOR IMMEDIATE RELEASE - , 201
CSPI: FDA should address raw shellfish
WASHINGTON, Feb. 9 (UPI) -- A non-profit group is urging the U.S. Food and Drug Administration to set a standard for the shellfish industry to reduce illnesses from eating raw shellfish. David W. Plunkett, a senior food safety attorney at the Center for
E-cigarettes will get FDA oversight as tobacco products - OrlandoSentinel.com
The Food and Drug Administration announced Monday that it will act to ensure the government's right to impose marketing, manufacturing and safety restrictions on "electronic cigarettes," a nicotine delivery device widely billed as an alternative to cigar
Cancer Drug Erases Alzheimer's Symptoms in Days
Alzheimer's Reading Room In the study described below, the cancer drug Bexarotene quickly and dramatically improved brain function and social ability and restored the sense of smell in mice bred with a form of Alzheimer's disease. Imagine this. Within ho
Generic insulin, cancer therapies? They're coming
Even as Republican presidential candidates vow to dismantle what they call "Obamacare" -- the Patient Protection and Affordable Care Act of 2010 -- some of the law's key provisions are making their way onto the medical landscape. The latest step toward i
News page is in maintenance. Sorry for the inconvenience.
Clear
Clear