Understanding Medical Device Regulatory Pathways in China and Japan

Release Date
July 20, 2017

To register for a recording of this webinar, please visit the Xtalks registration page.

The countries of China and Japan each present their own unique set of challenges pertaining to medical device development. This is especially true for foreign manufacturers as they strive to stay abreast of the quickly changing device regulations and product approval processes in these sometimes tough-to-navigate geographies.

Join us for a webinar with XTalks on July 20, 2017, as NAMSA’s regulatory experts Lei Yang, Medical Research Manager-China; and Kei Yoshikawa, Medical Research Manager-Japan, present information that will assist attendees to:

Time will also be allotted for Q&A.

To register for a recording of this webinar, please visit the Xtalks registration page.