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MEM has the expertise and procedures in place to assist our OEMs through the regulatory and validation process.

MEM's mission statement is :

We pride ourselves in achieving the highest quality standards and often exceed our customers' expectations.

Our quality system is certified to ISO 13485:2003 by BSI.


  • FDA Device Registered Facility
  • Class 10,000 (ISO 7) Certified Cleanrooms
  • Six Sigma Certified processes practiced


For a copy of our ISO certificate, click on image below.

ISO 13485-2003 Certificate Copy






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