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ISO 13485 Medical Devices Management Standard

Improved Risk Management and Quality

What are the benefits to your business in implementing ISO 13485?

Improved risk management and quality assurance
Meeting customer expectations and improved ability to respond to customer requirements
Increased efficiency and cost savings
Improved ability to win more business through proven business credentials
Help to maintain the quality of supply chain

10 real benefits of implementing ISO Management System;

ISO standards help you improve the quality of your goods and services
ISO standards help you drive growth, cut costs and increase profits
ISO standards give your business a competitive edge
ISO standards open up export markets for your goods and Services
ISO standards open doors to new customers and strengthen your existing business
ISO standards help you compete with bigger enterprises
ISO standards enhance your credibility and secure customer Confidence
ISO standards sharpen your business processes and increase efficiency
ISO standards strengthen your marketing pitch
ISO standards help you comply with regulation

Improve Business Performance

What is ISO 13485 Medical Devices Management System?

ISO 13485 is an internationally recognised standard that sets out requirements for a comprehensive management system for the design, development, manufacture, installation, and servicing of medical devices. It is often seen as the first step towards achieving compliance with European, Canadian and other regulatory requirements for medical device manufacturers. This system is essential for any organisation operating at any tier in the medical device supply chain.

Implementing this system means not only increased efficiency and cost savings but the improved ability to win more business through proven credentials.