Meet the Psephos Team

Mark has worked in the pharmaceutical and medical device industry since 2005 with a particular focus on Quality Management Systems, Quality Assurance and drug management for clinical trials. His activities included adherence to standards such as GDP (Good Document Practice), GCP (Good Clinical Practice), Quality Mangement systems (ISO 13485 and 21 CFR 820) and FDA regulation 21 CFR part 11 Electronic Records: Electronic Signatures.