By Richard Conforti, M.S., Nerac Analyst,
Originally Published: June 14, 2016
In 2014 the Chinese Food and Drug Administration, CFDA, updated their regulations on medical devices. These updates substantially changed the way in which a medical device company, particularly international companies not based or founded in China, registers their devices in China.
In part 2 of this 3 part series, the author discusses the changes to selecting clinical literature.
Want to read the rest of the article? Fill out the form to download:Understanding CFDA Expectations Regarding Clinical Literature Evaluation for Medical Devices under Order 650: A Nerac Perspective, Part II
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