As the gateway into Japan PMDA and China NMPA regulations for medical devices and IVD products, we are committed to your needs. i Access Consulting provides a wide-range of regulatory services across the full spectrum of product design and development to make a successful entry to the Japan and China medical device markets.

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        Having the right regulatory partner at the right time can be invaluable in attaining compliance and market access. i Access Consulting is the industry leader in driving successful regulatory submissions and outcomes through effective, daily interactions with the Japan PMDA, Notified Bodies and China NMPA.