保健食品注册审评审批工作细则（2016 年版）目 录1.总则....................................................................................................................51.1 制定依据......................................................................................................51.2 适用范围......................................................................................................51.3 工作原则......................................................................................................52.注册受理............................................................................................................52.1 材料审查......................................................................................................52.1.1 国产新产品注册申请材料....................................................................52.1.2 国产产品延续注册申请材料..............................................................102.1.3 国产产品变更注册申请材料..............................................................112.1.4 国产产品转让技术注册申请材料......................................................142.1.5 证书补发申请材料..............................................................................142.1.6 进口产品注册申请材料......................................................................152.2 材料补正....................................................................................................162.3 材料受理....................................................................................................162.4 材料移交....................................................................................................173.技术审评..........................................................................................................173.1 组织专家审查组........................................................................................173.1.1 专家审查组的组成......................................................................
