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Clinical Study
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Frutarom's New Clean Label Solution Combats Iron Deficiency in Vegetarians
Dec 15, 2015Frutarom Health BU offers a new approach to tackle iron deficiency in vegan and vegetarian diets. AB-Fortis, a patented encapsulated iron system, supports vegans/vegetarians, as well as women of childbearing years, who commonly suffer ...
Tags: Frutarom, Vegetarians, iron
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FDA's First Weight-Loss Device TP for Obese Adults to Dieting and Having Bariatric Surgery
Jan 19, 2015The EnterMedics Maestro Rechargeable System weight loss treatment device is effective although scientists are unclear why. The FDA has approved the first weight-loss device since 2007, giving obese adults an alternative to dieting and ...
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Ces with an Entire Array of New Technology and Devices That Sparkle
Jan 13, 2015This year, for the first time at CES, gadget makers got it right, with an entire array of new technology and devices that sparkle, shine, and made me seriously swoon. Here's what caught my eye: Mirror, Mirror on the Wall Panasonic's ...
Tags: CES 2015, Beauty Equipment
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The FDA Wants Medical Device Developers to Join Them in Facilitating a Smoother
Aug 20, 2014The FDA wants medical device developers to join them in facilitating a smoother, quicker approval process. A proposed Medical Device Development Tools qualification process would affect measurement tools that assess medical device ...
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Concurrent with This Acquisition, The Release of PharmaCM CT 2.0 Was Announced
Jun 9, 2014Consolidation in the clinical trials management software space recently took another step forward as the PharmaCM platform, along with substantially the rest of the assets of Deloitte Analytics LLC, became part of TrialScope Inc. ...
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FDA Approved Its Single- and Dual-Chamber Entovis Pacemakers for Use in MRI Environments
May 9, 2014FDA has approved its single- and dual-chamber Entovis pacemakers for use in MRI environments, according to Biotronik Inc. The Lake Oswego, OR–based US subsidiary of Biotronik SE & Co. KG (Berlin) said in a press release that its ...
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Heat-Processed Foods May Cause Brain Changes Similar to Alzheimer's Disease
Mar 10, 2014Heat-processed foods may increase risk of Alzheimer's Compounds commonly found in the so-called “Western diet” known as Advanced Glycation Endproducts (AGEs) may cause brain changes similar to Alzheimer’s disease and ...
Tags: Heat-Processed Foods, Foods
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The Low-Cost Neonatal Breathing System Increased The Survival Rate of Newborns
Feb 25, 2014The first clinical study of a low-cost neonatal breathing system created by Rice University bioengineering students demonstrated that the device increased the survival rate of newborns with severe respiratory illness from 44 percent to 71 ...
Tags: Respiratory Illness, premature babies, CPAP
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U.S. FDA Today Approved The Expanded Use of Blood Sugar Monitoring System
Feb 13, 2014February 3, 2014 -- The U.S. Food and Drug Administration today approved the expanded use of the Dexcom G4 Platinum Continuous Monitoring System for patients with diabetes ages 2 to 17 years. The G4 Platinum System, which monitors blood ...
Tags: FDA
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Edwards Received Regulatory Approval to Sell Sapien 3 Transcatheter Aortic Heart Valve
Feb 11, 2014Edwards Lifesciences has received regulatory approval to sell its third-generation Sapien 3 transcatheter aortic heart valve in Europe. Edwards Lifescience's Sapien 3 could be used in a broader range of patients than earlier TAVR ...
Tags: Sapien, Medtronic', CoreValve
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Miltenyi Biotec Receives Approval From FDA for Clinimacs CD34 Reagent System
Feb 10, 2014German biotechnology company Miltenyi Biotec has received the US Food and Drug Administration's(FDA)approval for its CliniMACS CD34 reagent system to prevent graft-versus-host disease(GVHD)in the treatment of acute myeloid leukemia(AML). ...
Tags: Miltenyi Biotec, Blood, Medicine
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Hetlioz Has Been Approved by The U.S. Food and Drug Administration
Feb 8, 2014Hetlioz (tasimelteon) has been approved by the U.S. Food and Drug Administration to treat a sleep condition caused by a completely blind person's inability to regulate the body clock by recognizing light from dark. The condition is ...
Tags: blind person's inability, new drug
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Patient Enrollment Was Completed by Venaxis in Appy1 Test Trial
Jan 26, 2014Venaxis, a US-based in vitro diagnostic firm, has completed the patient enrollment in its pivotal clinical study of the APPY1 test in the US. The APPY1 test, a unique appendicitis test, has projected high sensitivity and negative ...
Tags: Venaxis, APPY1, Steve Lundy, FDA
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U.S. FDA Today Approved The First Gel Sealant for Use in Stopping Fluid From Leaking
Jan 13, 2014The U.S. Food and Drug Administration today approved the first gel sealant for use in stopping fluid from leaking through the incision in a patient's cornea after cataract surgery with intraocular lens placement in adults. Prior to today's ...
Tags: Gel for Sealing Corneal Incision, First Gel After Cataract Surgery
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A Sealant Gel to Prevent Fluid Leakage
Jan 13, 2014A sealant gel to prevent fluid leakage after cataract surgery has been approved by the U.S. Food and Drug Administration. While gels such as ReSure have been approved to seal small incisions in other parts of the body, this is the first ...
Tags: Sealant Gel, Eye Surgery
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