Emergo Group Corp. of Austin, TX at MEDICA 2018 in Düsseldorf -- MEDICA - World Forum for Medicine

Emergo Group Corp.

2500 Bee Cave Road, Building 1, Suite 300, 78746 Austin, TX
USA

This company is co-exhibitor of
Messe Düsseldorf North America

Hall map

MEDICA 2018 hall map (Hall 16): stand D32-9

Fairground map

MEDICA 2018 fairground map: Hall 16

Our range of products

Product categories

  • 07  Medical Services and Publications
  • 07.10  Consulting services for health organisations

Consulting services for health organisations

  • 07  Medical Services and Publications
  • 07.15  Technical equipment management, test houses / certification bodies

Technical equipment management, test houses / certification bodies

  • 07  Medical Services and Publications
  • 07.16  Certification and testing of medical devices, quality assurance

Certification and testing of medical devices, quality assurance

Our products

Product category: Technical equipment management, test houses / certification bodies

Cybersecurity Risk Management and Procurement Support

ANSWERED ON THIS PAGE:

  • Have you identified cyber risks for your connected medical technology before bringing it to market?  
  • How do your risk management decisions impact your ability to complete procurement processes?
  • How can early cybersecurity assessments mitigate concerns, and delays to market, and facilitate regulatory compliance?

Cybersecurity risk is no longer relegated to computers and personal devices. Digital threats are part of any item with network connectivity, including medical devices. Our team can help you define your attack surface, attack vectors, and assets to be protected. We’ll help you identify those vulnerabilities that potentially impact functionality for users and outcomes for patients.

Aligning risk assessments for industry with regulatory and procurement requirements


A guidelines-based risk assessment will help you improve cybersecurity hygiene and speed to market of your devices. This includes evaluating and consulting on your products’ ability to meet the expectations of industry, regulators, Health Delivery Organizations, and Group Purchasing Organizations. Our risk assessments are based on the FDA-recognized UL 2900 standard and the National Institute of Standards and Technology

(NIST) Cyber Security Framework. The assessment will include:

  • Monitoring information sources to detect cyber vulnerabilities and risk
  • Identifying clinical performance to help develop protections and responses to cybersecurity risks
  • Recognizing methods to address risks prior to any occurrence

Product and supplier assessments to evaluate cybersecurity risks
Many companies invest considerable time and resources enhancing their cybersecurity measures. But if they fail to thoroughly assess all devices in their digital ecosystem, they can put the company, patients, and users at risk. Our team helps identify risks that may be introduced through your suppliers, technologies used in designing your devices, or to your technology infrastructure via procurement. Our supplier risk analysis considers:

  • Identification of potential assets, threats, and vulnerabilities,
  • Impact analysis of threats and vulnerabilities on device functionality and end users/patients,
  • Likelihood determination of a threat and/or a vulnerability being exploited.

Emergo provides cybersecurity risk assessments for procurement processes
Our knowledge of connected devices and cybersecurity regulations can help you control your procurement decisions and procedures against cyber threats. We understand where potential hardware and software vulnerabilities lie. Our team can support your efforts to demonstrate compliance with regulators expectations. Here’s how we can help:

  • UL 2900 FDA recognized standard compliance: Ensuring your device complies with FDA-recognized standards and guidance
  • Comprehensive cybersecurity risk assessment: Evaluate potential risks from the supplier and the devices/components in consideration
  • Build cybersecurity measures into procurement procedures: Establish purchasing protocols and documentation that address cybersecurity risks
  • Help identify your organization’s cybersecurity posture: Evaluate your organizations’ supply chain cybersecurity process maturity and establish a maturity model
  • Compliance and regulatory form submissions: Help compile the necessary cybersecurity documentation for device registration submissions
Please contact us for more information about procurement consulting on cybersecurity for network connected devices.

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About us

Company details

Emergo is Your Global Medical Device Compliance Partner
Emergo by UL is a leading regulatory consulting firm specializing in global medical device and IVD compliance. Our comprehensive solution is designed to help you achieve and maintain regulatory and commercial success. With a presence on six continents, we can provide real-time service and on-the-ground expertise. Learn more about how we can help you grow.

Expand your global reach through market compliance consulting
We help device companies meet registration requirements in the world’s biggest markets. With a team of experienced RA/QA consultants working across the globe, we can assist with device registrations, quality management system implementation, in-country representation, clinical study compliance, regulatory strategy, and more. Learn more about our approach to device market compliance.

Navigate cybersecurity risks with digital health consulting
Our team of digital health consultants can help you meet the regulatory and practical obligations of today’s network-connected healthcare space. We assist with regulatory documentation, risk assessments, procurement support, data privacy compliance, and more to mitigate the risk of cyber threats to your company. Learn more about digital health compliance.

Make better, safer products through human factors research and design
Our usability researchers and designers are among the best in the world. From building interactive prototypes to analyzing the root cause of an adverse event, we can help you achieve market success, meet regulator expectations, and reduce risk through superior design. Learn more about our approach to human factors research and design.

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