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23:54 EDT 22nd September 2017 | BioPortfolio

Transdermal Drug Delivery Technologies, Markets, and Companies [Report Updated: 08092017] Prices from USD $3500

Benefits of this reportUptodate onestop information on transdermal drug deliveryDescription of 110 companies involved and 110 collaborations in this areaMarket analysis 20152025/Market values in major regionsStrategies for developing markets for transdermal drug deliveryA selected bibliography of 220 publicationsText is supplemented by 22 tables and 14 figuresWho should read this report?Biotechnol...

Yes on Issue 2 Petitioner Denounces Big Drug Company Ad as Racist and Anti-Semitic

Yes campaign’s Tracy Jones calls on big drug companies to pull offensive ad off airwaves Tracy Jones, one of the original Yes on Issue 2 petitioners, called on the big drug companies and their campaign manager Curt Steiner to pull down their racist and anti-Semitic TV ads off the airwaves. The ads, which use the phrase “Michael Weinstein...

Agilent Technologies Receives Expanded FDA Approval for the Use of Dako PD-L1 IHC 22C3 pharmDx Companion Diagnostic in Gastric or Gastroesophageal Junction (GEJ) Cancer

Patients with gastric or GEJ adenocarcinoma whose tumors express PD-L1 can now be identified for potential treatment with KEYTRUDA® (pembrolizumab) using PD-L1 IHC 22C3 pharmDx Agilent Technologies Inc. (NYSE: A) today announced its Dako PD-L1 IHC 22C3 pharmDx assay has an expanded label approved by U.S. Food and Drug Administration (FDA), for use as ...

Supermarket Wellness Watch: Data shows breadth of retailer health commitments

David OrgelIn the latest installment of Supermarket Wellness Watch, David Orgel takes a deep dive into FMI’s report on food retailers’ health-and-wellness efforts — from pharmacy to dietitians to retail clinics.  read more

Statement from FDA Commissioner Scott Gottlieb, M.D., on FDA's immediate steps to respond to Hurricane Maria and ongoing recovery efforts related to Hurricane's Harvey and Irma

SILVER SPRING, Md., Sept. 22, 2017 /PRNewswire-USNewswire/ -- As the citizens of Puerto Rico and the U.S. Virgin Islands begin the long recovery effort from the devastation brought by Hurricane Maria, I know I'm joined by all of my colleagues at the Food and Drug Administration in keeping the residents of all these islands in our thoughts. I also want to extend my thanks to the FDA staff in o...

Mendelson, Werner join Drug Store News team

Industry trade publishing veterans Seth Mendelson and Steven Werner bring nearly 50 years of editorial and sales experience to the nation’s leading drug store publication. read more

SDM's new WellWise store will 'change the conversation on how people age'

Michael JohnsenWellWise breathes a little retail pizzazz into what has traditionally been a clinical retail shopping experience, Shoppers Drug Mart's Theresa Firestone told Drug Store News. read more

Criminal and civil actions filed against Aegerion Pharmaceuticals Inc.

SILVER SPRING, Md., Sept. 22, 2017 /PRNewswire-USNewswire/ -- Today, Aegerion Pharmaceuticals Inc. agreed to plead guilty in the United States District Court for the District of Massachusetts to two misdemeanor counts of violating the Federal Food, Drug, and Cosmetic Act (FD&C Act) involving the introduction of misbranded Juxtapid (lomitapide) into interstate commerce. In connection with this ...

Allergan Receives Refusal to File Letter from FDA for Vraylar® (cariprazine) Supplemental New Drug Application (sNDA) for the Treatment of Negative Symptoms in Schizophrenia

DUBLIN, Sept. 22, 2017 /PRNewswire/ -- Allergan plc (NYSE: AGN) today announced that it received a Refusal to File (RTF) letter from the U.S. Food and Drug Administration (FDA) regarding its Supplemental New Drug Application (sNDA) for Vraylar (cariprazine) for treatment of negative symptoms associated with schizophrenia in adult patients. VRAYLAR is an oral, once daily atypical antipsychotic appr...

What is Food Safety?

Take the Culture of Food Safety Quiz SOURCE: Essity (Formerly SCA) DESCRIPTION:National Food Safety Month was created in 1994 to heighten the awareness of food safety education. Each year, we feature a new theme and create free training activities and posters for the restaurant and foodservice industry to help reinforce proper food safety practices and procedures. Test your knowledge on the five c...

Janssen Receives Complete Response Letter From U.S. FDA For Sirukumab Biologics License Application

HORSHAM, Pa., Sept. 22, 2017 /PRNewswire/ -- Janssen Biotech, Inc. (Janssen) announced today that it has received a complete response letter from the U.S. Food and Drug Administration (FDA) for the Biologics License Application (BLA) seeking approval of sirukumab for the treatment of moderately to severely active rheumatoid arthritis (RA). The complete response letter indicates additional clinical...

European Food Safety Authority report on glyphosate herbicide copied parts of Monsanto document

Eleven Biotherapeutics Announces Completion of Vicinium Manufacturing for Ongoing Clinical Trials in Non-Muscle Invasive Bladder Cancer

-- Topline Three-Month Data from Phase 3 Registration Trial Expected in Mid-2018 -- Eleven Biotherapeutics, Inc. (NASDAQ:EBIO), a late-stage clinical oncology company advancing novel product candidates based on its Targeted Protein Therapeutics (TPTs) platform, today announced that it has completed the manufacturing of all Vicinium necessary for its ...

Norwalk company acquires South Carolina drug plant

GSK packages of Alli on display, with the drug having been manufactured at an Aiken, S.C. plant being acquired by Norwalk, Conn.-based Avara Pharmaceuticals for future use as an outsourced drug production and packaging facility in a deal announced Sept. 21, 2017.

Krystal Microplate Enables Development of Drug Testing Assay for Plasmodium vivax

Porvair Sciences reports that the National Center for Biological Sciences (NCBS) in Bangalore, India is using its Krystal 384 black microplate to produce a standard drug testing assay for Plasmodium vivax infection. The NCBS is a leading national institute whose faculty members undertake research in the frontier areas of biology. Scientists at the NCBS use experimental and computational approaches...

FDA approves bevacizumab biosimilar Mvasi

On 14 September 2017, the US Food and Drug Administration (FDA) approved its first biosimilar for the treatment of cancer.

Neogen announces management change

LANSING, Mich., Sept. 22, 2017 /PRNewswire/ -- Neogen Corporation (NASDAQ: NEOG) announced today that Richard E. Calk Jr., formerly president and chief operating officer, has resigned from the company to pursue alternative opportunities. Calk's duties have been assumed by John Adent, who will now serve as president and chief executive officer. Adent joined the company as chief executive ...

Abbott Secures FDA Approval for MRI-Compatibility for the Company's Ellipse™ ICD

ABBOTT PARK, Ill., Sept. 22, 2017 /PRNewswire/ -- Abbott (NYSE: ABT) today announced U.S. Food and Drug Administration (FDA) approval for magnetic resonance (MR)-conditional labeling for one of Abbott's most widely-used implantable cardioverter defibrillators (ICD) and associated high voltage leads. The approval of MR-conditional labeling for the Ellipse™ ICD with the Tendril MRI pacing lea...

FDA forms working group to increase generics competition

US Food and Drug Administration (FDA) Commissioner Dr Scott Gottlieb had announced the creation of a working group of senior staff focused on increasing generic drug competition.

Mallinckrodt Advocates for Comprehensive, Multi-Prong Action Plan to Fight Opioid Abuse and Misuse in the United States

ST. LOUIS, Sept. 22, 2017 /PRNewswire/ -- Mallinckrodt plc (NYSE: MNK), an industry leader in the effort to address prescription drug diversion and misuse in the United States, today outlined its "Prescription for America's Opioid Epidemic" – six integrated policy initiatives that the company believes, if implemented, would significantly advance the fight against prescription drug abuse and misu...

MuShield Company Earns Coveted AS9100 Certification

MuShield Company has achieved AS9100 Revision D certification - endorsed by all major aerospace regulators, including the Federal Aviation Administration (FAA), US Department of Defense (DoD), International Aerospace Quality Group (IAQG) and the National Aeronautics and Space Administration (NASA). Londonderry, New Hampshire (PRWEB) September 22, 2017 MuShield Company is very pleased to announce ...

ZEUS Scientific Announces U.S. FDA Premarket Approvals (PMA) and Launch of its ZEUS ELISA™ Parvovirus B19 Test Systems

Designed to significantly improve laboratory’s processing turnaround time and productivity with excellent precision and accuracy Branchburg, NJ, USA (PRWEB) September 22, 2017 ZEUS Scientific, a leading global diagnostic solutions company, today announced the launch of ZEUS ELISA Parvovirus B19 IgG and IgM Test Systems, following receipt of Premarket Approvals (PMA) from the U.S. Food and Drug ...

Cellectar, Onconova partner on cancer drug conjugates

An early-stage collaboration could boost the two small-cap biotechs' pipelines. 

Food 4 Less/Foods Co Charitable Campaign To Benefit Children's Hospitals

LOS ANGELES, Jan. 26, 2012 /PRNewswire/ -- Southern California based Food 4 Less is pleased to announce that it is raising funds to support children's hospitals in the communities its stores serve in Southern California, southern Nevada, and the greater Chicago area. In addition, the supermarket chain's Foods Co Division is collecting donations for children's hospitals in central and northern Cali...

Fast NMR Data Collection in 2D Explained in New Apps Note

JEOL’s ECZ series NMR is used in routine and cutting edge experiments in the fields of polymers, pharmaceuticals, food, batteries, and more.

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