New issue explores regulatory compliance strategies for the Chinese FDA, strategies for innovation and opportunities and challenges in desalination technologies.
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- 62November issue offers in-depth business perspectives on industry issues, compliance challenges and commercial opportunities authored by Nerac analysts Read the full release here.
- 56By Richard Conforti, M.S., Nerac Analyst, Originally Published: August 15, 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 the final…
- 56Gain a working knowledge of the clinical literature evaluation process for China in the Nerac webinar hosted by FX Conferences: Order 650 – China’s New CLE Requirements for Medical Devices Click here to register. In 2014 the Chinese FDA updated its regulations for medical devices, Order 650, under which manufacturers are now required to perform…