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The FDA: Food and Drug Administration or Fairy Dust Alliance? Are You Really Being Protected 1 year 6 weeks ago

Is the Food & Drug Administration Really Protecting You or is it All a Fairy Tale?

"Since its conception in 1906, the Food and Drug Administration has been viewed as the ultimate authority on food safety, by people all across the nation. Much to the dismay of many, the smoke, mirrors, and fairy dust being cast out by this organization is beginning to wear off of the formerly trusting, dreamy-eyed consumers and their true power, or lack there of, is being exposed. According to www.expertrecall.com:

Things Looking Up for Lilly and Acrux: The FDA Approves Men’s Sex Drug 1 year 25 weeks ago

Things are looking up for Eli Lilly and Co. and Acrux—the US Food and Drug Administration (FDA) has just approved their testosterone topical solution. Axiron, a replacement therapy for men with low testosterone levels, is the first testosterone topical solution approved for application via an underarm applicator.

FDA vitamins and supplements 2 years 3 weeks ago

FDA stands for Food and Drug administration. FDA, or known as USFDA, is a health and human services department in the United States. The manufactures do not need FDA approval for vitamins and supplements to be sold. There are a lot of vitamin food supplements out on the market. Getting the best quality of vitamins, minerals, and dietary supplements can sometimes be difficult.

FDA rejection for Biodel Linjeta NDA 1 year 29 weeks ago

The U.S. Food and Drug Administration (FDA) has issued a complete response letter (CRL) to Biodel stating that its Linjeta new drug application (NDA) cannot be approved in its present stage. In the CRL, the FDA demands additional information with respect to the Linjeta (human insulin [rDNA origin]) injection 100IU/ml NDA for the treatment of type 1 and type 2 diabetes mellitus to enhance glycemic control.

Ethicon Endo-Surgery appeals FDA for Sedasys system 1 year 28 weeks ago

Ethicon Endo-Surgery (EES) is urging the Office of the Commissioner of the Food and Drug Administration (FDA) to grant the company’s appeal of the Center for Devices and Radiological Health’s (CDRH) denial of the Sedasys System premarket approval application (PMA).