Food and Drug Administration Newswire (Page 8)

Food and Drug Administration Newswire (Page 8)

Comprehensive Real-Time News Feed for Food and Drug Administration. (Page 8)

Results 141 - 160 of 142,296 in Food and Drug Administration

  1. Interesting book on the pharmaceutical industryRead the original story w/Photo

    Monday | HEALTH'Sass

    First, a disclaimer. I have not read the whole book--and am excerpting from a story on it.

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  2. SpineGuard Receives FDA Clearance to Market Its DSGa Integration...Read the original story w/Photo

    Monday | Business Wire

    ... to make spine surgery safer, announced today it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its new DSGa (Dynamic Surgical Guidance) integration module to be used in combination with Zavation's spinal fusion ...

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  3. Donor Allegedly Pushed Staff to Help GOPBy Kaiser Health NewsRead the original story w/Photo

    Monday | The Daily Beast

    ... of legal restrictions on employer coercion. The email arrived as Petit publicly pressed the Food and Drug Administration to change its stance on the regulation of MiMedx products, which could potentially affect the company's bottom line or lead to a ...

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  4. The Future Five: Innovations We Might See in 2017 or in the Very Near FutureRead the original story w/Photo

    Monday | Customer Interaction Solutions

    Just a few years ago, minimally invasive surgery to treat serious conditions such as stroke and heart valve defects was unimaginable. But technology has brought us to the point where such patients can be treated quickly and safely through intravenous microsurgery, often walking around within hours and leaving the hospital in just a few days.

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  5. Manufacturer Issues Security Updates to Fix Pacemakers that Can Be HackedRead the original story w/Photo

    Monday | Personal Injury News

    St. Jude Medical has issued security updates for its Merlin remote monitoring system, which are designed to fix flaws that could make its pacemakers vulnerable to hacking. According to a report in the Washington Times, certain pacemakers, defibrillators and other products manufactured by St. Jude are reportedly vulnerable to "cyber security intrusions and exploits," the U.S. Food and Drug Administration warned consumers.

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  6. Fake Viagra brings convenience store crackdownRead the original story w/Photo

    Monday | St. Petersburg Times

    The U.S Food and Drug Administration is warning consumers about tainted male enhancement products that could pose health risks. They're typically sold at convenience stores or gas stations.

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  7. Blog: FDA Issues Discussion Paper on Laboratory Developed TestsRead the original story w/Photo

    Monday | JD Supra

    The U.S. Food and Drug Administration issued today a Discussion Paper on Laboratory Tests . The Discussion Paper follows draft guidance issued by the FDA in 2014 and a stakeholder workshop held in 2015 regarding the oversight of LDTs.

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  8. Shareholder Alert: Bronstein, Gewirtz & Grossman, LLC Notifies...Read the original story w/Photo

    Monday | GlobeNewswire

    ... Complaint further suggests that on September 17, 2015, TG Therapeutics announced that the U.S. Food and Drug Administration (FDA) had contacted them due to a Special Protocol Assessment on the make of a Phase 3 clinical trial for TG-1101 and ...

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  9. BOLT System offers management solution to meet new food-handling regulationsRead the original story w/Photo

    Monday | Trucker

    ... as canned items, and milk products already regulated under other rules, are exempt. The U.S. Food and Drug Administration adopted the rules earlier this year to enforce the Food Safety Modernization Act, which Congress approved and President Obama ...

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  10. What sorts of toxics are lurking in your lipstick, eyeliner?Read the original story w/Photo

    Monday | The Columbian

    ... their use in this manner They are not designed, tested or approved for this use." In 2010, the Food and Drug Administration, which oversees some aspects of cosmetic safety, asked Frontier Global Sciences Inc. to test 400 lipsticks for lead ...

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  11. Could This Study Could Be Disastrous for Marijuana Stocks?Read the original story w/Photo

    Monday | Fox News

    ... is beneficial for treatment of chemotherapy-induced nausea and vomiting. In July 2016, the U.S. Food and Drug Administration (FDA) approved Insys Therapeutics ' oral cannabinoidSyndros for this indication based on clinical study data. It would ...

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  12. New Technology May Change Treatment for the Foot and AnkleRead the original story w/Photo

    Monday | Axcess News

    For those suffering from osteoarthritis or knee injuries, a new technology may help you move better and have less pain. Agili-C is a cartilage and bone regeneration device that actually helps your body regrow on its own.

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  13. Building a 21st Century FDARead the original story

    Monday | Isegoria

    A 2010 study in the Journal of Clinical Oncology by researchers from the M.D. Anderson Cancer Center in Houston, Texas found that the time from drug discovery to marketing increased from eight years in 1960 to 12 to 15 years in 2010. Five years of this increase results from new regulations boosting the lengths and costs of clinical trials.

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  14. P-Cure says it can beam tumors away at half the costRead the original story w/Photo

    Monday | The Times of Israel

    ... two additional ones at a private hospital in London this year. The product received US Food and Drug Administration (FDA) clearance in August. P-Cure has also reached a collaboration accord with Philips Healthcare for a joint development of a ...

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  15. How Much Milk Can You Squeeze Out of an Almond?Read the original story w/Photo

    Monday | MousePrint.org

    ... for filing a claim is April 13, 2017. Last November, 25 members of Congress wrote to the Food and Drug Administration calling on the agency to investigate and take action against any producers of "milk" products that are not derived from cows. And ...

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  16. FDA Wants More Time to Review Eli Lilly-Incyte's BaricitinibRead the original story

    Sunday | BioSpace

    ... and Company (NYSE: LLY) and Incyte Corporation (NASDAQ: INCY) announced today that the U.S. Food and Drug Administration (FDA) has extended the review period for the new drug application (NDA) for investigational baricitinib, a once-daily oral ...

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  17. Alert: Physio-Control's Defibrillator Has Shut Down Unexpectedly During Patient TreatmentRead the original story

    Sunday | BioSpace

    ... or events associated with the use of a Physio-Control product may be reported to the U. S. Food and Drug Administration's MedWatch Safety Information and Adverse Event Reporting Program online at www.fda.gov/MedWatch/report.htm , by phone ...

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  18. Sunovion Release: Biopharma Announces Pivotal Study Results For Novel ...Read the original story

    Sunday | BioSpace

    ... Washington, D.C. Pending successful completion of ongoing studies and discussions with the U.S. Food and Drug Administration (FDA), Sunovion intends to submit a New Drug Application (NDA) to the FDA in 2017 for ADHD in children and adults. "Sunovion ...

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  19. SafeOrthopaedics Release: Company Announces The Commercial Launch Of...Read the original story

    Sunday | BioSpace

    ... and associated single-use ancillary) has also received (510k) marketing approval from the US Food and Drug Administration (FDA). Although it is not commercialized in the United States, this technology will gain more rapid approval in certain ...

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  20. Tocagen Release: Company Expands Toca 5, Phase II/III Clinical Trial...Read the original story

    Sunday | BioSpace

    ... lung, breast, renal and melanoma. Tocagen obtained Fast Track designation from the U.S. Food and Drug Administration for Toca 511 & Toca FC as a treatment of recurrent HGG and Orphan drug designation for the treatment of glioblastoma multiforme ...

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