Quality Policy

MIM Software Inc. is committed to developing safe, reliable, innovative, and user-friendly software products for the medical imaging community. Our goal is to provide exceptional imaging technology and image management to support diagnosis and treatment, which will in turn result in better patient outcomes.

Our employees strive to provide quality products and superior technical support based on the quality management system we have implemented. Our quality management system meets the requirements of the FDA Quality System Regulation,the ISO 13485:2016 standard, and other international regulatory regulations and standards required of medical device manufacturers prior to international sale.

Executive management ensures that this policy is:

  • Suitable to the organization.

  • Communicated to and understood by all employees.

  • Periodically reviewed to ensure that the effectiveness of the quality management system is maintained.

Certifications and Licenses:

  • US FDA Cleared Software

  • Certified to ISO 13485:2016

  • Certified to Medical Device Directive 93/42/EEC (CE 0120)

  • Health Canada Medical Device License

  • Australian Register of Therapeutic Goods (ID: 236191)

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