What is an FDA Calendar? Biotech investing is risk-fraught, as stocks are at the mercy of several catalysts – most of which are make-or-break events, aka binary events. A prudent investment ...

Genetic Apex Emblem Event 1 is the first PvP event running in Pokémon TCG Pocket. While we've already seen a Wonder Pick and player versus AI event, this one will truly test your TCG Pocket ...

The emblem of a red cross on a white background is a sign of protection under the Geneva Conventions. It is not a religious symbol. The red cross, red crescent and red crystal are symbols of ...

Kennedy Jr., who is slated to hold a potentially big role in a new Trump administration, said Wednesday there are “entire departments” within the Food and Drug Administration (FDA) that ...

FDA to review if there's a shortage of tirzepatide Outsourcing Facilities Association lawsuit led to FDA reconsideration Shortages of Lilly and Novo Nordisk drugs drive demand for compounded ...

The Food and Drug Administration approved a drug produced by AbbVie for the treatment of late stage Parkinsons disease the company announced Thursday. The regulator approved Vyalev, also known as ...

The Food and Drug Administration is issuing exemptions from the Drug Supply Chain Security Act’s current final implementation deadline for some drug manufacturers and distributors, according to ...

Oct 17 - The U.S. Food and Drug Administration has approved Avadel Pharmaceuticals' (AVDL.O), opens new tab sleep disorder drug for children aged 7 years and older, broadening its use and heating ...

The FDA periodically inspects facilities that manufacture dietary ... Dietary supplements that have gone through third-party testing will typically include the certification emblem on their packaging.

In order to receive the GHNA emblem, products must meet nutrition criteria informed by the latest evidence-based nutrition authoritative guidance from the 2015-2020 Dietary Guidelines for Americans, ...

UGN-102 could become the first FDA-approved medicine for the treatment of low-grade intermediate-risk non-muscle invasive bladder cancer (LG-IR-NMIBC). The FDA has assigned a Prescription Drug ...

BERLIN--(BUSINESS WIRE)--Bayer today announced that the U.S. Food and Drug Administration (FDA) has accepted the company’s New Drug Application (NDA) for the investigational compound ...