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Federal Register

Rule Removes Vaccine Mycoplasma Testing

Federal Register notice: FDA issues a final rule to remove the specified test for detecting the presence of Mycoplasma for live virus vaccines and ina...

Human Drugs

FDA Allows Controversial Convalescent Plasma for Covid

In a swirl of Trumpian controversy, FDA issues an emergency use authorization for Covid-19 convalescent plasma and its use in treating hospitalized Co...

Medical Devices

HelixBind Gets Breakthrough for Sepsis Test

FDA awards HelixBind a breakthrough device designation for its RaPID/BSI, a direct-from-blood platform for identifying and characterizing bloodstream ...

Human Drugs

Complete Response in Tricida Metabolic Acidosis NDA

FDA issues Tricida a complete response letter on its NDA for veverimer, a non-absorbed, orally-administered polymer designed to treat metabolic acidos...

Medical Devices

Valencia Tech PMA for Bladder Electrical Stimulation

Valencia Technologies files a PMA for its eCoin Peripheral Neurostimulator System for use in treating overactive bladder.

FDA General

Since Our Last Issue ...

Industry news you may have missed since our last issue.

Federal Register

Study Data Tabulation Model Notice Corrected

Federal Register notice: FDA corrects a notice that appeared in the 7/7 Federal Register that discussed version 1.7 of the Clinical Data Interchange S...

Human Drugs

CBERs Marks Would Resign on Premature Vaccine Approval

CBER director Peter Marks says he would resign if the Trump Administration interfered in an approval decision to speed up access to a premature Covid-...

Federal Register

Regulatory Review Period for Oxervate

Federal Register notice: FDA determines for patent extension purposes the regulatory review period for Dompe Farmaceuticis Oxervate (cenegermin-bkbj)....

Federal Register

Public Meeting on CDER Standard Core Sets

Federal Register notice: FDA announces an 8/28 virtual public meeting entitled Public Meeting on CDER Standard Core Sets: Clinical Outcome Assessments...