Medical Engineering Technologies (Dover, U.K.) announced that it has appointed Kevin Claris as the company’s new manager for Good Manufacturing Practice and ISO 17025 documentation.
He will be working with the company’s technical and quality team to develop new training programs.
Claris has more than 30 years of experience in cGMP environments. Prior to joining Medical Engineering Technologies, Claris worked with Pfizer and Mylan in mostly manufacturing environments. He also has experience in implementing quality systems and has been involved in the development of bronchodilators and the accompanying MHRA FDA submissions.
Medical Engineering Technologies’s labs specialize in design validation testing of drug delivery devices.
