What is ISO 13485 Certification? What is 21 CFR 820 Compliance?

Why implement a QMS system?

  1. · Increase access to more markets worldwide with certification.
  2. · Outline how to review and improve processes across your organization.
  3. · Increase efficiency, cut costs, and monitor supply chain performance.
  4. · Demonstrate that you produce safer and more effective medical devices.
  5. · Meet regulatory requirements and customer expectations

Harmonize the requirements of ISO 13485:2016 & 21 CFR part 820 and open new opportunities for your business further.

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Email – enquiry@mavenprofserv.com

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