Search form
Search
contact us
Navigation
home
boards
Jobs
job ratings
cp wire
medtech news
pharmagather
catering
advertise
whistleblower info
pharmaceutical fraud
medical device | DME fraud
clinical lab fraud
False Claims Act
Legal Help
login/register
You are here
Home
»
companies
» FDA
FDA
Pear claims breakthrough tag for alcohol use disorder DTx
Pharmaforum
Wed, 11/24/21 - 10:04 am
digital health
Pear Therapeutics
breakthrough device
devices
reSET-A
alcohol-use disorder
FDA
Aadi clinches first FDA nod for ultrarare sarcoma drug Fyarro
Fierce Pharma
Tue, 11/23/21 - 08:54 pm
Aadi Bioscience
Fyarro
sarcoma
FDA
Why FDA Boosters Authorization Could Be More Important for Pfizer and Moderna Than You Might Think
Motley Fool
Tue, 11/23/21 - 10:01 am
FDA
Pfizer
Moderna Therapeutics
vaccines
boosters
COVID-19
New drug applications pile up with delays as there's no easy fix for the inspection backlog
Endpoints
Tue, 11/23/21 - 09:52 am
FDA
regulatory
inspections
pandemic
COVID-19
Buoyed by new data, Santhera preps filing for DMD drug vamorolone
Pharmaforum
Tue, 11/23/21 - 09:43 am
Santhera
DMD
Duchenne Muscular Dystrophy
idebenone
vamorolone
FDA
House COVID-19 panel seeks interview with former Trump FDA leader Hahn
The Hill
Mon, 11/22/21 - 10:21 pm
Stephen Hahn
FDA
Donald Trump
COVID-19
vaccines
FDA shakes up hepatitis C testing market by opening up 510(k) pathway
Medtech Dive
Mon, 11/22/21 - 10:30 am
FDA
regulatory
diagnostics
hepatitis C
510(k)
Bluebird bio may finally get a gene therapy approved in the US
Endpoints
Mon, 11/22/21 - 10:28 am
Bluebird Bio
gene therapy
FDA
Zynteglo
beta-thalassemia
priority review
Gilead files first hepatitis delta therapy with FDA
Pharmaforum
Mon, 11/22/21 - 10:25 am
Gilead Sciences
buleviritide
antivirals
hepatitis delta
FDA
FDA asks for 55 years to complete FOIA request on Pfizer's COVID-19 vaccine | FiercePharma
Fierce Pharma
Sat, 11/20/21 - 12:03 pm
Pfizer
vaccines
COVID-19
FDA
FOIA
BioNTech Bags Fast-Track Status for Melanoma Treatment
BioSpace
Sat, 11/20/21 - 11:56 am
BioNTech
melanoma
BNT111
FDA
fast track
FDA expands emergency authorization for Covid-19 booster shots to all adults
Stat
Fri, 11/19/21 - 11:15 am
FDA
Moderna Therapeutics
Pfizer
BioNTech
vaccines
COVID-19
boosters
Emergency Use Authorization
FDA delays its decision on Bristol Myers' $13B heart drug another three months
Endpoints
Fri, 11/19/21 - 11:08 am
Bristol Myers Squibb
FDA
ICER
mavacamten
obstructive hypertrophic cardiomyopathy
FDA approves first drug for genetic cause of dwarfism
Stat
Fri, 11/19/21 - 11:06 am
Biomarin
FDA
dwarfism
achondroplasia
Voxzogo
Three Pharma Companies Seek to Address FDA Rejections
BioSpace
Wed, 11/17/21 - 11:50 pm
FDA
Iterum
sulopenem
Eton Pharmaceuticals
Acadia Pharmaceuticals
Nuplazid
Medtronic Leadless Pacemaker Linked to Major Complication Risk
Medical Devices and Diagnostics Industry
Wed, 11/17/21 - 11:48 pm
Medtronic
devices
FDA
leadless pacemakers
Micra
cardiac perforation
FDA grants first approval for a VR system to treat chronic lower back pain
Fierce Biotech
Wed, 11/17/21 - 11:43 pm
FDA
low back pain
virtual reality
devices
Medtech
EaseVRx
AppliedVR
F.D.A. Plans to Authorize Pfizer Boosters for All Adults This Week
NY Times, NY
Wed, 11/17/21 - 11:25 pm
Pfizer
COVID-19
vaccines
boosters
FDA
Moderna asks FDA to approve boosters for all adults
Beckers Hospital Review
Wed, 11/17/21 - 11:19 pm
Moderna Therapeutics
COVID-19
vaccines
FDA
boosters
Does biopharma support the Califf nom for FDA? Yeah, whatever
Endpoints
Wed, 11/17/21 - 10:31 am
FDA
regulatory
Robert Califf
Pages
« first
‹ previous
…
95
96
97
98
99
100
101
102
103
…
next ›
last »