account...that RTA 402 has been granted orphan drug designation by the U.S. Food and Drug Administration (FDA ...
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PHARMACEUTICAL APPROVALS
Pharmaceuticals approvals are the last step in a long process of government testing. This topic tracks the approval of prescription and over-the-counter pharmaceuticals.
Pharmaceutical Approvals is part of Business Exchange, suggested by
Evan Rappaport.
This topic contains
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314 blog
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Read updated news, blogs, and resources about Pharmaceutical Approvals. Find user-submitted articles and reactions on Pharmaceutical Approvals from
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Blogs
Recent blog posts on this topic.
Health and agriculture departments in all 50 states will have rapid access to FDA's Recall Enterprise System by Sept.
...even if the drug is not indicated for use in a pediatric population. In fact, if the drug ... By John R.
Sponsors, and Monitors. Designed for clinical investigators, clinical site staff, study monitors, regulatory affairs...
(M2) The U.S. Food and Drug Administration (FDA) has increased inspections and product testing efforts in response to...
...in loosening marketing restrictions and reducing product liability for drug and device makers...
This past August the FDA released a study of 324 women's and children's vitamins and their lead levels.
(Dân trí) - Các nhà chức trách tại Mỹ đã cảnh báo người dân không được sử dụng 7 loại cà phê tan và trà sữa có
But the FDA did not reveal this risk to doctors and hospitals that were considering participation in future studies,...
26 (HealthDay News) -- As food-safety problems continue to rock the United States, resulting in massive recalls,...
The FDA recently gave KJAYA Medical approval to market the firm's image reconstruction solution, utilizing proprietary...
Read full story for latest details.
The willful blindness of the Food and Drug Administration (FDA) - its ... declines in new drug approvals, which will
...in a patient taking Genentech and Biogen Idec's blockbuster arthritis and cancer drug Rituxan.
PGx & Molecular Dx...
Uwe Kunkel and Michael Radke. Web Release Date: Sat, 30 Aug 2008 00:00:00 EDT (Article) DOI: 10.1021/es801562j
Pathwork Diagnostics, Inc., a molecular diagnostics company focused on oncology, announced that the U.S.
Eisai received a "not approval" letter from the FDA for its proposed sedative for patients who need minimum...
[link][comments]
...clinical trial application has been conditionally approved by the U.S. Food and Drug Administration (FDA).
The next two to four years are an important time frame for many pharmaceutical companies. It is when many of the top...
...it reached a deal to buy U.S. generic drug maker APP Pharmaceuticals in ... in the deal, along with a registered and...
...leading manufacturer of multi-source and branded injectable pharmaceutical products, today announced that it has...
FDA's drug review and drug safety offices have set aside their differences and laid out an agreement that more equally...
Top Sources: Pharmaceutical Approvals
- SeekingAlpha.com: Home Page
- DODTracker.com New Deals Feed
- stockerblog.blogspot.com
- What's New at CBER
- RSS from PharmiWeb.com
- futurebiopharma.blogspot.com
- In the Pipeline
- FDA Law Blog
- Health News from Medical News Today
- Medical Device Recalls since November 11, 2009
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Senior Manager  Global Governance in Drug Development and Medical, Strategy & Business Operations
EMD Serono
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Billerica, MA
Posted: Apr 23
Occupational Health Nurse For Dsm Pharmaceuticals
Vidant Medical Center
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Greenville, NC
Posted: May 15
Executive Pharmaceutical Sales Specialist (San Diego/Orange County, CA)
Shire Pharmaceuticals
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Field, KY
Posted: May 18
