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China to speed up drug approvals, will accept overseas trial data
October 9, 2017 / 4:37 AM / 2 months ago

China to speed up drug approvals, will accept overseas trial data

SHANGHAI, Oct 9 (Reuters) - China is looking to speed up approvals for new drugs and plans to accept data from clinical trials carried out overseas, a potential boon for international drugmakers and patients who often face lengthy delays for new medicines to reach the market.

The move, announced by the Cabinet late on Sunday, said foreign drug trial data would be accepted in a bid to accelerate approvals and help China close an innovation gap with developed international markets.

“Clinical trial data from overseas centres that complies with Chinese drug and medical device registration requirements can be used to make registration applications in China,” the draft proposals posted on the State Council’s website said.

Generally, draft proposals announced in China are later implemented much as they first appear.

The move should help speed up approvals in the world’s second largest drug market, after the United States, where global firms have faced rising challenges from Chinese rivals and authorities are keen to squeeze down prices.

The proposal said that firms looking to register drugs or medical devices for the first time would need to provide clinical trial data related to any racial divergence relevant to the Chinese market.

The announcement comes as China aims to boost its drug industry and support a shift from generic drugs and towards more innovative medicines and medical equipment - a trend that raises a longer-term challenge to global firms.

The State Council added that the changes would make China’s industry more competitive and help meet the clinical needs of its nearly 1.4 billion people, for whom high costs and access to healthcare are significant issues.

“Overall, China’s support for scientific innovation with drugs and medical devices is lacking, and the quality of products on the market still falls short of top international levels,” the central government body said.

“We must speed up the examination and approval of urgently needed drugs and medical devices,” it added. (Reporting by Adam Jourdan; Editing by Richard Borsuk)

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