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Food and Drug Administration Company Profile

13:20 EDT 21st September 2018 | BioPortfolio

In 2006, FDA commemorates the 100th anniversary of its founding law, the 1906 Pure Food and Drugs Act. FDA is the oldest consumer protection agency in the nation.

Location

5600 Fishers Lane
Rockville
Maryland
20857
United States of America

Contact

Phone: 1-888-463-6332
Email: combination@fda.gov


News Articles [3123 Associated News Articles listed on BioPortfolio]

The US Food and Drug Administration’s tentative approval process and the global fight against HIV

This paper was originally published by Harinder Singh Chahal, Jeffrey S Murray, Martin Shimer, Peter Capella, Ryan Presto, Mary Lou Valdez, and Peter G Lurie in Journal of the International AIDS… T...

Genetron Healths' biochip reader GENETRON 3D had received the approval for launch to facilitate ...

BEIJING, Aug. 22, 2018 /PRNewswire/ -- At the end of 2017, Chongqing Food and Drug Administration of China Food and Drug Administration (CFDA) officially approved Read more...

Alnylam Receives Orphan Drug Designation from the United States Food & Drug Administration for ALN-TTRsc02

Alnylam Pharmaceuticals (Nasdaq: ALNY), the leading RNAi therapeutics company, announced today that the United States Food and Drug Administration (FDA) has granted Orphan Drug Designation to ALN-TTR...

FDA staff raises safety concerns over Lilly/Incyte arthritis drug

An experimental rheumatoid arthritis drug developed by Eli Lilly and Co and Incyte Corp poses serious risks of deadly blood clots at higher doses, U.S. Food and Drug Administration staff said on Thurs...

US Food and Drug Administration Approves ARAKODA™ (tafenoquine) tablets for oral use; First preve...

60° Pharmaceuticals (60P) announced today the Food and Drug Administration (FDA) approval of ARAKODA™ (tafenoquine) tablets for the prevention of malaria in patients aged 18 years and older.

Postmarket studies required by the US Food and Drug Administration for new drugs and biologics approved between 2009 and 2012: cross sectional analysis

AbstractObjectivesTo characterize postmarketing requirements for new drugs and biologics approved by the US Food and Drug Administration (FDA), and to examine rates and timeliness of registration,... ...

White House proposes a narrowing of FDA’s mission — and a new name

The Trump administration has proposed a fundamental change to the mission of the Food and Drug Administration, one that would transfer most of the responsibility for regulating food safety to…

Lipocine Receives Complete Response Letter for Tlando From U.S. Food and Drug Administration

SALT LAKE CITY, May 9, 2018 /PRNewswire/ -- Lipocine Inc. (NASDAQ: LPCN), a specialty pharmaceutical company, announced today that it has received a Complete Response Letter ("CRL") from the United St...

PubMed Articles [5068 Associated PubMed Articles listed on BioPortfolio]

US Food and Drug Administration Disruption of Generic Drug Market Increases Hospital Costs.

The purpose of the US Food and Drug Administration's Marketed Unapproved Drugs Initiative is to decrease marketing of older unapproved medications. The administration has recently extended its rulings...

Electrocardiogram Monitoring After the Food and Drug Administration Warnings for Citalopram: Unheeded Alerts?

To evaluate national trends in electrocardiogram (EKG) monitoring in Veterans Affairs (VA) beneficiaries prescribed high-dose citalopram before and after the 2011-12 Food and Drug Administration (FDA)...

Anticipating Industry Arguments: The US Food and Drug Administration's Authority to Reduce Nicotine Levels in Cigarettes.

The US Food and Drug Administration has announced that it is considering lowering nicotine levels in cigarettes to "minimally addictive or nonaddictive levels." This could be a transformative public h...

A 25-Year Experience of US Food and Drug Administration Accelerated Approval of Malignant Hematology and Oncology Drugs and Biologics: A Review.

Accelerated approval (AA) is a US Food and Drug Administration (FDA) expedited program intended to speed the approval of drugs and biologics that may demonstrate a meaningful advantage over available ...

Drug-Associated Acute Kidney Injury Identified in the United States Food and Drug Administration Adverse Event Reporting System Database.

Acute kidney injury (AKI) is a common condition associated with both short-term and long-term consequences including dialysis, chronic kidney disease, and mortality. Although the United States Food an...

Clinical Trials [6167 Associated Clinical Trials listed on BioPortfolio]

Bioequivalence Study of Levothyroxine Sodium Tablets 150 mcg

The objective of this study is to establish the bioequivalence of two levothyroxine formulations through the estimation of T4 levels in serum samples after baseline correction, according t...

A Study to Evaluate the Use of the Drug Combination Vorinostat, Niacinamide, and Etoposide in Patients With Lymphoid Malignancies That Have Reoccurred

The purpose of this study is to test the safety of a combination of two anticancer medicines, called vorinostat and etoposide, with a high dose of a vitamin called niacinamide. These medic...

Study to Evaluate Bioavailability of Apremilast Oral Suspension Relative to Tablet and a Study to Assess Effect of Food on the Pharmacokinetic (PK) of the Oral Suspension

The purpose of this study is to assess how much of apremilast is found in the blood unchanged when administered as an oral suspension compared to when it is administered as a tablet formul...

Genetic Predictors of Variability in the Drug-Drug Interaction Between Darunavir/Ritonavir and Pravastatin

Pravastatin (Pravachol) is approved by the Food and Drug Administration (FDA) and is used to treat high cholesterol. Darunavir (Prezista) and ritonavir (Norvir) are approved by the Food a...

An Open-Label, Randomized, Comparative 3-Way Cross-Over Study to Evaluate the Effect of Food on the 24-Hour Intragastric pH at Day 5 After Twice Daily Oral Administration of PN 200 (Omeprazole/Naproxen) in Healthy Volunteers

Primary: To compare the pharmacodynamic efficacy of PN 200 in controlling intragastric pH (percent time pH> 4.0) following twice daily administration at different dosing times relative to ...

Companies [2653 Associated Companies listed on BioPortfolio]

Food and Drug Administration Alumni Association, Inc.

The Food and Drug Administration Alumni Association, Inc. is an educational, service-orientedorganization founded in 2001 by a small group of FDA retirees and employees. The non-profit,non-lobbying or...

Food and Drug Administration

In 2006, FDA commemorates the 100th anniversary of its founding law, the 1906 Pure Food and Drugs Act. FDA is the oldest consumer protection agency in the nation.

Avatar Corporation

Avatar Corporation is a manufacturer and distributor of raw materials and ingredients for the food, drug, and cosmetic industries. We are a privately held, Illinois corporation. Our principal offices ...

U.S. Food and Drug Administration

Privia

A clinical trial is a research study. Research studies are used to decide how treatments work and how safe they are. While in a study, a person may receive either an investigational drug, a marketed d...

More Information about "Food and Drug Administration" on BioPortfolio

We have published hundreds of Food and Drug Administration news stories on BioPortfolio along with dozens of Food and Drug Administration Clinical Trials and PubMed Articles about Food and Drug Administration for you to read. In addition to the medical data, news and clinical trials, BioPortfolio also has a large collection of Food and Drug Administration Companies in our database. You can also find out about relevant Food and Drug Administration Drugs and Medications on this site too.

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Food is any substance consumed to provide nutritional support for the body. It is usually of plant or animal origin, and contains essential nutrients, such as carbohydrates, fats, proteins, vitamins, or minerals. The substance is ingested by an organism ...


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