Medical Engineering Technologies Appoints New GMP Manager
We are very pleased to announce the appointment Kevin Claris as Manager for Good Manufacturing Practice and ISO 17025 documentation, here at MET.
Kevin has 30 years experience of working in cGMP environments. He has pursued his career with both Pfizer and Mylan. This work has mostly been in manufacturing environments. As well as having a great deal of experience in the implementation of quality systems, Kevin has been involved in the development of bronchodilators and their associated MHRA and FDA submissions.
Kevin has a particular interest in training and will also be working with the MET technical and quality teams to further develop our training programmes
Our laboratories specialise in design validation testing of drug delivery devices. Contact our team to find out more about performance testing, drug stability and compatibility, or extractables and leachables studies.