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By FDAzilla
Today, FDAzilla unveiled Enforcement Analytics, a ground-breaking data analytics tool that gives industry greater insights into FDA enforcement actions and inspection activity.
By Cure SMA
The SMA drug pipeline has grown dramatically in just over a decade. Of the 17 programs in the pipeline, seven of these are in clinical trials, and two of those are in Phase 3 clinical trials.
By Applied Spectral Imaging Inc.
Carlsbad, CA. – April 16, 2015 – Applied Spectral Imaging (ASI, announced today that it has received clearance from the South Korean Ministry of Food and Drug Safety (MFDS) for its GenASIs HiPath image capture and analysis...
By E-QURE Corp
Dr. Sessler, is an MD that has gained proficiency and 20 years experience in business development and marketing.
By VEXTEC Corporation
The Food and Drug Administration (FDA) will evaluate VEXTEC’s Virtual Life Management (VLM®) for certification as a Medical Device Development Tool (MDDT).
By Ross Medical Corporation
New control center platform and device offers continuous real-time ECG monitoring and cardiac event detection for patients receiving a hospital like workup in the community.
By Visiongain
London, UK, 12th of February 2015: A new report by visiongain predicts that the world pre-filled syringes and pen injectors/autoinjectors market will reach $4.3bn in 2015.
By calabasas dental institute
CALABASAS, Calif. —  The Federal Drug Administration has issued a new warning on graft substitutes containing recombinant proteins or synthetic peptides.
By Applied Spectral Imaging Inc.
FDA Clearance for GenASIs™ HiPath IHC Family for HER2, ER, PR and Ki67
By American Conference Institute
The American Conference Institute (ACI) is proud to announce that its industry leading FDA Boot Camp conference is returning to New York City on March 10-11, 2015.
NAAFA, BEDA and believe that forcing chain restaurants to include caloric value of every dish and drink on their menus is a wasted effort and could be counterproductive.
By Online Compliance Panel
This webinar will focus on the commonly cited accreditation surveyor citations for facility operations, and what could be done to avoid these citations by facility administrators and managers
By Online Compliance Panel
This webinar will begin by studying the timeline of events in interpreting these events to show the chain of actions and their impact leading to deteriorating state of control and potential injunctive action.
By Datex Corporation
Supply chain software developer Datex Corporation announced new pharmaceutical editions of its award winning warehouse management software for the pharmaceutical, medical device and life sciences industries.
By Datex Corporation
Datex Pharmaceutical Software now includes a suite of features which enables compliance of the new FDA regulation, the Drug Quality Security Act (DQSA).  The FDA Drug Quality and Security Act (DQSA) was signed into law in late 2013.
By Critical Path Institute
The Critical Path Institute (C-Path) announced today that the U.S.
By FDAnews
9th Annual FDA Inspections Summit **Presented by FDAnews** Oct. 22-24, 2014 – Bethesda, MD
By marcus evans
Inviting Heads, VPs, Directors, Managers, and Specialists of Labeling and Regulatory Affairs from leading pharmaceutical and biotech companies to discuss best practices for generic label documentation
By SanRx®
SanRx Advances Development as Part of Collaboration with Northwest Clinical Research Center in Bellevue, Wa.
By Chemic Laboratories Inc.
Chemic Laboratories Inc. and Brenntag, a global market leader in chemical distribution, today announced the establishment of a formal three-year Joint Cooperation Agreement.
By American Conference Institute
American Conference Institute (“ACI”) is pleased to announce that the 3rd FDA & USDA Compliance Boot Camp, taking place at the InterContinental Chicago Magnificent Mile on September 29-30, 2014 will feature senior government officials from the...
By Public Interest Law Professor John Banzhaf
The WHO has just recommended very tough restrictions on e-cigarettes, including a total ban on their use in public places, regulations to ensure the products contain a standard dose of nicotine, and a ban on sales to children and the use of flavors
By American Conference Institute
American Conference Institute (ACI) is proud to announce that its industry leading FDA Boot Camp conference is returning to Boston, MA on September 18-19, 2014.
By Alliance for Natural Health USA
Deceptive Labeling Confuses Consumers and Contradicts State Department Policies
By Alliance for Natural Health USA
FDA guidelines are unconstitutional, violate the First Amendment and the Equal Protection Clause, and contravene Congressional intent.
By RxforAmericanHealth
A stance by the Pharmaceutical Research and Manufacturers of America (PhRMA) for the U.S.
By Cambridge Healthtech Institute
Bringing Industry, Academia and Regulatory Authorities Together to Produce Safe and Efficacious Products for the Clinic and Beyond
By TodaysSeniorsNetwork
HHS Secretary urged to act to block needless destruction of safe, authentic personally imported prescription medicines
By Q1 Productions
Social Media Implications, Solidifying Data for On-Site Presentation Among Key Topics
This seminar is designed for professionals in in the Medical Device, Pharmaceutical, and Biotech startup companies

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