medical device

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Published By: UL     Published Date: Dec 04, 2019
From its first documented use nearly 30 years ago, robotics today is playing a major role in efforts to bring innovative patient treatments to the healthcare industry. Robotically assisted equipment and systems are now being widely used in advanced surgical procedures, helping to reduce complications and improve overall surgical outcomes. The International Electrotechnical Commission (IEC) has now published a standard to address the specific performance and safety characteristics of robotically assisted equipment. The standard, IEC 80601-2-77, Medical Electrical Equipment – Particular requirements for the basic safety and essential performance of robotically assisted surgical equipment, bridges an important gap in previously available medical device standards. Reflecting more than a decade of work by industry experts from around the world, IEC 80601-2-77 is expected to be adopted in the near future by regulatory authorities in most international medical markets for use in assessing the
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UL
Published By: UL     Published Date: Dec 04, 2019
Risk of electromagnetic interference and immunity have long been important in the evaluation of the safety of medical devices by regulatory authorities. But the expanded scope of environments in which medical devices are being used today, along with the growing prevalence of all types of medical and non-medical systems and devices utilizing wireless communications technologies, new challenges have been created for medical devices and increased potential risks to patients.
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UL
Published By: UL     Published Date: Dec 04, 2019
Information on electrical safety, regulatory requirements and Electromagnetic Compatibility (EMC) Hosted by EMC expert, Bob DeLisi, the webinar will provide healthcare providers and manufacturers with expert information regarding electrical safety, compliance and EMC healthcare and medical devices. Topic covered will include: General changes to IEC 60601-1-2 Emissions testing Immunity testing Reporting
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UL
Published By: UL     Published Date: Dec 04, 2019
Information on electrical safety and regulatory requirements for laboratory equipment Hosted by Walter Hofmair, Principal Engineer at UL Munich, the webinar will provide healthcare providers and manufacturers with expert information regarding electrical safety and compliance for healthcare and medical device laboratory equipment. Topic covered will include: Overview of IEC 61010 particulars and specific requirements Changes in the new IEC 61010-3.1 IEC 61010 compliance
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UL
Published By: StoryDesk     Published Date: Mar 28, 2012
How can you use the iPad in your organization? What's the formula for a successful iPad deployment? What do you need to know about regulatory requirements, security, HTML5, and custom apps?
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enterprise applications
    
StoryDesk
Published By: Larsen & Toubro Infotech(LTI)     Published Date: May 30, 2019
Leading medical devices company were facing business continuity post acquisition, thereby increasing maintenance costs accordingly. LTI proposed to implement Oracle Fusion Cloud which helped in faster and minimal requirement of technical manpower. Benefits i. In-time Delivery with ZERO defects ii. Scalable products with low maintenance costs Download full case study.
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Larsen & Toubro Infotech(LTI)
Published By: Maetrics     Published Date: Oct 08, 2015
Re-evaluating Their Importance Under a New Regulatory Spotlight Every medical device sold into Europe, irrespective of its classification, must have an up-to-date Clinical Evaluation Report (CER) as part of its Technical File.
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Maetrics
Published By: Dassault Systèmes     Published Date: Nov 12, 2019
The Life Sciences industry has changed significantly over the past 10 years. With a view to developing new, more effective treatments, industry leaders are exploring new therapeutic areas and approaches like biologics and precision medicine. To address this shift, pharmaceutical and medical devices manufacturers look to connect systems, people and data - characterized by more predictive and adoptive facilities that leverage machine learning, 3D modeling, Industrial Internet of Things (IIOT), digital twin, and augmented reality. This eBook explains the main challenges of manufacturing and explores 5 manufacturing experiences that disrupt the future of manufacturing in the Life Sciences industry.
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iiot, medical device, life sciences, machine learning, 3d modeling, digital twin
    
Dassault Systèmes
Published By: UL EduNeering     Published Date: Jul 05, 2012
Cost reduction is a key criteria that executives often use when choosing initiatives to focus on. They are the ones that have the greatest potential to impact an organization's bottom line. Across life science organizations, a critical area for cost containment is training management.
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fda, gmp, gcp, gxp, cms, osha, qsr, 21 cfr part 11
    
UL EduNeering
Published By: UL EduNeering     Published Date: Jul 05, 2012
This paper summarizes the results of a quantitative benchmarking survey to over 200 Life Science organizations. The study identifies the key compliance and performance improvement training topics they had addressed in 2011 along with key issues for 2012.
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fda, gmp, gcp, gxp, cms, osha, qsr, 21 cfr part 11
    
UL EduNeering
Published By: UL EduNeering     Published Date: Jul 05, 2012
SOPs are critical to efficient manufacturing operations, quality control, and regulatory compliance. This paper reviews best practices for the Life Science industry for training on SOPs, and how learning management technology has the potential to improve learner retention through automated assessments.
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fda, gmp, gcp, gxp, cms, osha, qsr, 21 cfr part 11
    
UL EduNeering
Published By: UL EduNeering     Published Date: Jul 05, 2012
Third party intermediaries have played starring roles in some of the most highly publicized global corruption trials. By any measure, third party intermediaries routinely rank high on the list of compliance worries for brand companies.
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fda, gmp, gcp, gxp, cms, osha, qsr, 21 cfr part 11
    
UL EduNeering
Published By: UL EduNeering     Published Date: Jul 05, 2012
Good Manufacturing Practices (GMP) violations have become the new healthcare fraud as the Department of Justice (DOJ) tests out new legal theories under the False Claims Act (FCA). The Food and Drug Administration (FDA) has dusted off its regulatory authority to prosecute GMP violations.
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fda, gmp, gcp, gxp, cms, osha, qsr, 21 cfr part 11
    
UL EduNeering
Published By: Extreme Networks     Published Date: Feb 23, 2017
ABI Research’s Securing Medical Devices Technology Analysis Report analyzes the current risks posed by medical devices, noting various security issues, potential vulnerabilities, and the threat landscape. It reviews implementation mechanisms and efforts in medical device cybersecurity and safety. The final section looks at how the healthcare ecosystem is responding to the issues and the vendors driving change.
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abi. healthcare, cybersecurity, medical
    
Extreme Networks
Published By: Extreme Networks     Published Date: Feb 23, 2017
The network has never been as critical to the healthcare sector as it is today. Electronic health records, Wi-Fi-connected medical devices, and clinician smart phones are among a plethora of healthcare technologies that depend on a stable network. The consistent development of this infrastructure is key for the healthcare sector to continue its successes in creating new possibilities for management, patient and family experience, and patient outcomes. Extreme Networks posed key questions to Nolan Greene, a senior research analyst with IDC’s Network Infrastructure group, who highlights the critical issues healthcare IT professionals must consider when building a network that maintains industry needs. Download this report to learn about: • Why having a modern healthcare infrastructure is so important • The major challenges IoT brings to healthcare networks • How IEC 80001 is impacting compliance • Trends that confront a network IT professional in healthcare • Risks Healthcare IT must eli
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healthcare, iot, iec 800001, extreme networks, healthcare it
    
Extreme Networks
Published By: Akamai Technologies     Published Date: Mar 15, 2016
The globalization of the medical device industry has delivered substantial business benefits, but it has also presented certain problems that can make the realization of those opportunities challenging. Learn about a comprehensive global collaboration solution that addresses and overcomes these obstacles.
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medical device industry, global network, employee management, best practices, internet performance, internet security
    
Akamai Technologies
Published By: Intel     Published Date: May 19, 2017
For today’s service providers and enterprises, bandwidth demands continue to increase and evolve. The introduction of Internet of Things (IoT) solutions, such as smart homes, smart cities, connected cars, and connected medical devices, is forcing organizations to change existing business models and to build more cost-effective networks.
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nfv, enterprises, service providers, internet of things
    
Intel
Published By: UPS     Published Date: May 24, 2017
For life sciences businesses, the supply chain used to mean one thing: getting products from factory or warehouse to distributors or ultimate customers as quickly and economically as possible. Now, with today’s evolving regulatory environment, an increasingly globalized market, more complex health products, and an increased focus on the patient, pharmaceutical companies and medical device manufacturers are looking at their supply chain and logistics needs in a whole new way.
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health care, supply chain, ups, business, science
    
UPS
Published By: Larsen & Toubro Infotech(LTI)     Published Date: Mar 28, 2019
Leading medical devices company were facing business continuity post acquisition, thereby increasing maintenance costs accordingly. LTI proposed to implement Oracle Fusion Cloud which helped in faster and minimal requirement of technical manpower. Download complete case study.
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Larsen & Toubro Infotech(LTI)
Published By: GetWellNetwork, Inc.     Published Date: Nov 22, 2013
Learn how to improve the efficiency of your pain management workflow and see how these changes will improve the day to day tasks for your nurses allowing them to work more effectively.
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getwell network, pain management, pain management workflow, joint commission, pain assessment documentation, pain management workflow, performance improvement, managing patient pain levels
    
GetWellNetwork, Inc.
Published By: Pure Storage     Published Date: Oct 09, 2017
Semiconductors run and connect today’s technology-driven world, powering all the electronic systems and products around us. Critical to communication, entertainment, work, medical diagnoses, travel, socializing, and making new discoveries, these specialized chips are ubiquitous. And chip designs grow ever more sophisticated in order to power new generations of devices, computers, the Internet, and the cloud. To enable new applications and use cases – like the Internet of Things – semiconductor vendors have continually pushed the boundaries of their designs to accommodate new fabrication processes that make chips smaller, more power efficient (to make personal devices last longer), and able to pack more gates into smaller dies (to make them more powerful).
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verification, storage, customer, innovation, management, pure storage
    
Pure Storage
Published By: ETQ     Published Date: Jul 10, 2019
The FDA has announced plans to transition to standard ISO 13485:2016 for medical devices in 2019. In addition, the Medical Device Single Audit Program, MDSAP, has gained traction with full implementation set for 2019. Download this paper to learn more about these two changes from the U.S. Food and Drug Administration’s proposal to harmonize and modernize its Quality System Regulation (QSR).
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ETQ
Published By: Intel     Published Date: Feb 28, 2019
Digital transformation and smart technologies are paving the way towards smarter healthcare. Medwel understands that the goal of smart hospital development stems from the needs of the patient. By tapping on ICT advancements in the healthcare environment, the common goal is to reduce medical errors and achieve a holistic approach centered on the patients’ needs. Read more about the new MEDS-P1001—a 10.1” medical grade touchscreen PC that boosts • Effective computing through low power consumption • Interoperable through dual OS for different applications in hospitals • Health insights based on smart interfaces of vital sign measuring devices • Expandable functions through peripheral devices such as cameras, RFID reader, WIFI, etc. • Refined and reliable design that is slim, lightweight, antibacterial, water and dust-proof
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Intel
Published By: RES Software     Published Date: Jul 06, 2012
Today's IT managers face tough challenges. There's pressure to reduce IT costs, end user demand for flexible yet secure working, and the constant need to maintain regulatory compliance. Join the IT managers around the world who are solving their biggest challenges with RES Software. Learn how organizations in every sector are giving end users the freedom to work the way they want, in any location and via multiple devices, while drastically reducing demand for hands-on IT professionals.
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technology, res software, healthcare, desktop, healthcare it, medical device, it management, desktop migration
    
RES Software
Published By: MobileIron     Published Date: Aug 27, 2015
This is a case study about the Varian Medical system's focus on energy and saving lives through advanced technology.
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mobileiron, medical devices, medical software, security
    
MobileIron
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