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Mr. Locke has been in the invitro diagnostic medical device sector for 20+ years, has held senior level management positions, as a Global Director of Regulatory Affairs, Quality Management & Clinical Affairs. At Safeguard, Mr. Locke is responsible for Regulatory Affairs and Quality Compliance with his extensive experience in global regulations/standards to include MDD/IVDD, MDR/IVDR, US FDA CFR, CMDR/CMDCAS, ISO and post Brexit UK regulations.