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FDA delays updated \'nutrition facts\' relaunch

2017-07-05 21:13:00| Label and Narrow Web Breaking News

The deadline for which the food industry must comply with the new labeling will be pushed back for an undisclosed time.

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FDA Tells Soap Maker to Clean Up Its Website

2017-06-28 13:44:00| Happi Breaking News

Soapwalla has 15 days to fix its product claims.

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FDA Issues First Warning Letter in Since February

2017-06-19 20:33:00| Happi Breaking News

Agency cites Salt Lake City, UT skin care company for drug claims on its website.

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04/25/12 -- Helping The Dairy Industry Meet New FDA Food Handling Requirements

2017-02-08 05:52:19| dairynetwork News Articles

04/25/12 Dairy Network.com Newsletter

Tags: meet food industry requirements

 

FDA Accepts Two sBLAs for Mercks KEYTRUDA (pembrolizumab) for Locally Advanced or Metastatic Urothelial Cancer in Cisplatin-Ineligible First-Line and Second-Line Post-Platinum Failure Treatment Settings

2017-02-03 12:45:00| Merck.com - Product News

Dateline City: KENILWORTH, N.J. KEYTRUDA Also Receives Breakthrough Therapy Designation for Second-Line Treatment Based on KEYNOTE-045, Which Includes Primary Endpoints of Overall Survival and Progression-Free Survival KENILWORTH, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has accepted for review two supplemental Biologics License Applications (sBLAs) for KEYTRUDA (pembrolizumab), the companys anti-PD-1 therapy, in patients with locally advanced or metastatic urothelial cancer, a type of bladder cancer. Language: English Contact: For MerckMedia:Pamela Eisele, 267-305-3558orCourtney Ronaldo, 908-236-1108orInvestors:Teri Loxam, 908-740-1986orAmy Klug, 908-740-1898 Ticker Slug: Ticker: MRK Exchange: NYSE @Merck read more

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