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Description
A spin-off from ARQon in 2019 to provide one stop solution to customers for the advisory in the development of medical devices, from design control to commercialization in the following:
• Regulatory Technical documentation ie Design History File, Device Master Record, Device History record
• Production and Validation advisory, as well as contract manufacturing sourcing
• Quality Management System and Risk management
• Commercialization and distribution advisory
• Other client needs in education with IMDS program & training