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Medical Device Solutions

Medical Device Solutions

Moving your daily business operations to the "cloud" gives you the speed and flexibility you need to manage your business with precision. Bring your device to market more quickly and easily with InfoStrength's powerful document, project and quality management tools. These tools set you up for successful communications with the FDA and global regulatory bodies, regardless of where you are in the commercialization process. Med device companies use InfoStrength to:

  • Prepare 510(k) submissions for FDA approval
  • Meet 21 CFR Part 820 standards for cGMP and QMS
  • Gain a competitive advantage by managing ISO Certification
  • Utilize a business software that maintains validation compliance
  • Manage IEC 60601-1 safety testing requirements
InfoStrength users also benefit from:
  • Access to experienced regulatory and quality management consultants
  • No infrastructure to set up or maintain
  • Customized solutions that can be configured in hoursナ not weeks
  • Real time visibility of all your projects with project and team reports
  • 360ᄎ view of key business processes
  • Improved collaboration for your employees and vendors
  • Hardware and hosted computing environment management
To learn more about how InfoStrength can support your business, contact us today.
Contact InfoStrength