Our background in auditing medical device Quality Management Systems (QMS) means that we can implement or improve your QMS in line with best practices.
We have expert knowledge of ISO 13485 and making sure that you meet the requirements, but in a way that works for you. By utilising a pragmatic approach we can ensure that you get your medical device QMS working with you, not against you.
The ISO 13485 standard is an effective solution to meet the comprehensive requirements for a QMS. If you are seeking software to help take your QMS to the next level, we have partnered with GreenlightGuru.com, the only Quality Management Software designed speciﬁcally for the medical device industry.
Contact us today to see how we can help transform your QMS.