China, India Revamp Regulations for Medical Device Companies

China’s State Food & Drug Administration and India’s Drug Controller General of India have each revamped and released regulations governing medical device operations in their countries, according to a Healthpoint Capital report.

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The SFDA’s new rules require strict adherence to labeling and packaging guidelines as well as documentation for patient safety. The DCGI will take a similar approach and practice heightened scrutiny over medical device companies’ business practices.

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