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Food and Drug Administration Company Profile

18:26 EDT 17th June 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 [3167 Associated News Articles listed on BioPortfolio]

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...

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,... ...

Pfizer, Exelixis cancer drugs get FDA approval for wider use

Cancer treatments from Pfizer Inc and Exelixis Inc on Tuesday won approval from the US Food and Drug Administration for expanded use in previously untreated patients. The headquarters of the US Food a...

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...

FDA approves Mylan's copy of Allergan's vaginal cream

Mylan NV said the U.S. Food and Drug Administration had granted it the approval for a generic version of Allergan's Estrace cream for vaginal atrophy. FILE PHOTO: A view shows the U.S. Food and Dr...

AbbVie's Upadacitinib Granted Breakthrough Therapy Designation from the U.S. Food and Drug Administration for Atopic Dermatitis

NORTH CHICAGO, Ill., Jan. 8, 2018 /PRNewswire/ -- AbbVie (NYSE: ABBV), a global research and development-based biopharmaceutical company, today announced the U.S. Food and Drug Administration (FDA) gr...

Gene editing regulations threaten sustainability of global food animal supply

(Mary Ann Liebert, Inc./Genetic Engineering News) The US Food and Drug Administration's 2017 draft guidance that proposed drug-like regulatory scrutiny of food animals produced using gene editing tech...

PubMed Articles [4956 Associated PubMed Articles listed on BioPortfolio]

Social Media Impact of the Food and Drug Administration's Drug Safety Communication Messaging About Zolpidem: Mixed-Methods Analysis.

The Food and Drug Administration (FDA) issues drug safety communications (DSCs) to health care professionals, patients, and the public when safety issues emerge related to FDA-approved drug products. ...

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...

Transparency and Dermatologic Device Approval by the US Food and Drug Administration.

The US Food and Drug Administration approves Class III medical devices via the premarket approval pathway, often requiring clinical data on safety and efficacy. Manufacturers can submit incremental de...

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 ...

Magnitude of Clinical Benefit of Cancer Drugs Approved by the US Food and Drug Administration.

It is uncertain whether drugs approved by the US Food and Drug Administration (FDA) have clinically meaningful benefit as determined by validated scales such as the European Society for Medical Oncolo...

Clinical Trials [5828 Associated Clinical Trials listed on BioPortfolio]

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 ...

Use of Pyridostigmine for Constipation in Diabetics

Doctors at Mayo Clinic are doing this study to learn if pyridostigmine, a drug, affects the speed at which food travels through the stomach, intestines and colon, and if pyridostigmine imp...

Companies [2636 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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