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Quality Management

quality managementThe management system incorporated into the day-to-day operations here at MLE complies with the requirements of BS.EN.ISO 9001:2000 and ISO 13485:2003.

We have a very broad experience of various quality standards and processes required for different market places. Not only are our design and manufacturing processes approved and audited to ISO9001, we have achieved Scope extension to this quality standard to allow us to specifically design software. This process is audited by Tick-IT inspectors.

We continuously improve our Quality Management System and therefore the quality of the products and services we provide. Additionally our management system complies with ISO 13485:2003 for medical devices. This gives our medical device clients the certainty that their products are designed, developed and manufactured to the highest standards.

 

It is our policy to:

• Involve all employees in the quality improvement process realising every person has a responsibility to this.

• Provide an environment that promotes growth, motivation and fun.

• Provide outstanding products and services that exceed the clients' expectations.

• Develop constructive and mutually beneficial relationships with clients and suppliers.

• Aim to complete every task right first time with an emphasis on prevention of problems rather than relying on detecting them.

The Quality Policy is communicated throughout the organisation by means of every MLE employee or consultant having read and understood the Quality Management manual. The continuing suitability and application of this policy statement is reviewed at regular Management Review meetings.

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