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medical device Press Releases

SMARTdrill 6.0 Now Available for Orthopedic Surgery

SMARTdrill 6.0 Now Available for Orthopedic Surgery

The SMARTdrill 6.0 has been listed with the FDA and is now available in the United States for some of the most common orthopedic surgical procedures. Smart Medical Devices Inc. (SMD) will introduce the SMARTdrill 6.0 in the coming weeks.  “I…

Human Plasma on Demand; Velico Medical FrontlineODP System

Sunrise Labs, a medical device engineering firm, is proud to announce its collaboration with Velico Medical, Inc., of Beverly, MA, for the development of a life-saving technology; The FrontlineODP™ (On Demand Plasma) system for spray drying human plasma. FrontlineODP enables…

Spinal Singularity Receives ISO 13485:2016 Certification

Spinal Singularity has received ISO 13485:2016 certification. ISO 13485 is an international standard that sets the requirements for a comprehensive quality management system for the design and manufacture of safe and effective medical devices. High levels of safety and quality…

Nobilis Therapeutics Announces IND Filing for a Phase IIb Clinical Trial of NBTX-001 Drug/Device Combination for Treatment of Posttraumatic Stress Disorder

Nobilis Therapeutics Announces IND Filing for a Phase IIb Clinical Trial of NBTX-001 Drug/Device Combination for Treatment of Posttraumatic Stress Disorder

Nobilis Therapeutics, a biopharmaceutical company focused on the advancement of innovative CNS therapies, today announced that it has filed an Investigational New Drug application (IND) with the U.S. Food & Drug Administration (FDA) to initiate a Phase IIb clinical trial…

Nobilis Therapeutics Enters Into Collaboration With The Linde Group to Support Its Clinical Research Program to Study a Drug/Device Combination for Treatment of PTSD and Other CNS Disorders

Nobilis Therapeutics Enters Into Collaboration With The Linde Group to Support Its Clinical Research Program to Study a Drug/Device Combination for Treatment of PTSD and Other CNS Disorders

​Nobilis Therapeutics, a biopharmaceutical company focused on the advancement of innovative Central Nervous System therapies based on the use of noble gas mixtures, today announced that it has entered into a collaboration with The Linde Group to support its ongoing…

Designing Reliable Medical Devices by Solving Common Interconnect Challenges, New Webinar Hosted by Xtalks

Designing Reliable Medical Devices by Solving Common Interconnect Challenges, New Webinar Hosted by Xtalks

Individuals take for granted everyday interactions with well-designed products and devices that save both time and aggravation. Well-designed products can eliminate overall confusion for the user. Every day, more medical devices are designed for portability and at home monitoring. A…

5 Signs You Need to Re-Evaluate Your Clinical Trial Management and Simple Steps to Improve Efficiency, New Webinar Hosted by Xtalks

5 Signs You Need to Re-Evaluate Your Clinical Trial Management and Simple Steps to Improve Efficiency, New Webinar Hosted by Xtalks

​As clinical trials grow in complexity, managing trial operations becomes increasingly more burdensome on resources and more susceptible to risk and decreased efficiency. Evaluating your organization’s current process for managing clinical trials is the first step in determining if it’s…

How to Develop a Global Clinical Study Budget Like a Pro, New Webinar Hosted by Xtalks

How to Develop a Global Clinical Study Budget Like a Pro, New Webinar Hosted by Xtalks

Clinical research is a notoriously cost-sensitive industry. The Tufts Center for the Study of Drug Development estimated the average cost of bringing a new drug to market to be over $2 billion – and with clinical trial costs on the…

Simplifying Clinical Data Flow From EDC to SDTM, New Webinar Hosted by Xtalks

Simplifying Clinical Data Flow From EDC to SDTM, New Webinar Hosted by Xtalks

In a live webinar taking place on Thursday November 29, 2018 at 1pm EST, industry experts will discuss the challenge of simplifying clinical data flow from EDC to SDTM and offer some solutions. Recent trends in clinical trials - including…

Spinal Singularity to Present at the MedTech Strategist Innovation Summit

Spinal Singularity, a developer and marketer of innovative treatments for bladder management, today announced that Bill Colone, Chief Executive Officer, will present at the upcoming MedTech Strategist Innovation Summit: Burlingame, Nov. 27-28, at the Hyatt Regency San Francisco Airport. Mr. Colone…

Assembling the eClinical Suite: Taking Advantage of the Latest Technology While Avoiding Vendor Lock-Ins, New Webinar Hosted by Xtalks

Assembling the eClinical Suite: Taking Advantage of the Latest Technology While Avoiding Vendor Lock-Ins, New Webinar Hosted by Xtalks

Not all eClinical applications are the same. For one thing, an eTMF, an EDC and a CTMS all fulfill different functions. Perhaps more importantly, they are all built with varying degrees of complexity. The eTMF and EDC are both relatively simple…

BioBridges Appoints Joshua Nelson as a Director of Client Services

BioBridges Appoints Joshua Nelson as a Director of Client Services

BioBridges, a Career Portfolio® Management company providing integrated services to the life sciences community, is proud to announce and welcome Joshua Nelson as a Director of Client Services. Nelson will collaborate with emerging and established pharmaceutical, biotech, and medical device…

Medical Device Development: Using Advanced Simulation Technologies and Computer-Aided Engineering to Accelerate Time to Market, New Webinar Hosted by Xtalks

Medical Device Development: Using Advanced Simulation Technologies and Computer-Aided Engineering to Accelerate Time to Market, New Webinar Hosted by Xtalks

The potential for proactive use of simulation and computer-aided engineering (CAE) in medical devices is huge: saving lives and saving millions of dollars for the industry. This is accomplished by optimizing designs for performance and reliability, reducing the number of…

EU MDR Strategies: How to Achieve a Market Advantage While Streamlining Regulatory Compliance, New Webinar Hosted by Xtalks Sponsored by Kalypso

The European medical device industry is undergoing a transformation as the new European Medical Device Regulation is set to replace Medical Device Directives (93/42/EEC) and Active Implantable Medical Device Directive (90/385/EEC) by 2020. The European Union Medical Device Regulation (EU…

6 Ways to Combat the Problem of Counterfeit Drugs, New Webinar Hosted by Xtalks

Counterfeit drugs are a $200 billion business in the US, with an estimated one in every ten pharmaceutical products sold around the world being a fake. As well as the obvious financial toll counterfeit drugs place in the pharmaceutical industry,…

5 Critical Questions Small to Mid-Sized Sponsors Need to Ask When Evaluating an EDC Provider, New Webinar Hosted by Xtalks

Starting up a new study or successfully completing one study phase and advancing to the next can be a challenging time for sponsors. Choosing the right electronic data capture (EDC) provider to partner with plays an important role with downstream…

Pfizer and Bracket – How to Apply Patient-Centric Concepts to All Stages of Clinical Trials, New Webinar Hosted by Xtalks

Let’s move beyond the protocol and unlock the power of your study conduct before, during, and after your trial: Before: Additional advantages of pre-trial planning During: Cutting-edge tools and tactics to optimize the patient experience After: Post-trial gratitude and community…

Applying the Latest Digital Technology Trends to Patient, Provider and Payer Communications, New Webinar Hosted by Xtalks

Have you wondered how the Internet of Things (IoT) will impact healthcare and pharmaceutical communications? If you are curious about the latest digital trends and how that innovation is being implemented into real-world communication needs, don’t miss this live webinar…

Inhalation Drug Delivery: Considerations for Toxicology and Pharmacology Research, New Webinar Hosted by Xtalks

Drug delivery to the lungs in both the clinical and non-clinical setting is a unique combination of formulation, delivery device and the system/model that the drug is being delivered to. Throughout different stages of drug development, the requirements for inhalation…

Crack the Code: 3 Defining Steps to Unlock Medical Technology Commercialization Potential

Telos Partners, LLC, together with First Security Bank and Accelerate Montana, present: “Crack the Code:  3 Defining Steps to Unlock Medical Technology Commercialization Potential” Embarking on the journey of commercializing medical technology can be an ominous and daunting task, with questions regarding regulation,…

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