《关于进一步改革完善药品生产流通使用政策的若干意见》针对药品生产领域的六方面改革意见,综合来看实际上是通过提高注册、质量、节能、环保、安全生产等标准,严格市场准入,形成市场倒逼机制,同时也给指出了相应的企业转型“明道”。药品上市审评审批改革实质上是通过审评审批影响未来药品市场增量, Several Opinions on Further Reforming and Perfecting the Policy on the Use of Drugs in Production and Circulation In light of the six opinions on reform in the field of pharmaceutical production, in actual fact, we have adopted strict standards of market access such as registration, quality, energy conservation, environmental protection and safety in production, Forced market mechanism, but also pointed out that the corresponding corporate restructuring “Ming Road ”. Review of drug listing approval review and approval reform in essence is through the review and approval of the future drug market increases,