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劣质药品投诉到卫生健康委员会。【本文所涉及的法律依据】::《中华人民共和国药品管理法》 第一百零三条 药品监督管理部门应当对药品上市许可持有人、药品生产企业、药品经营企业和药物非临床安全性评价研究机构、药物临床试验机构等遵守药品生产质量管理规范、药品经营质量管理规范、药物非临床研究质量管理规范、药物临床试验质量管理规范等情况进行检查,监督其持续符合法定要求。
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certificate for holding of firearms for official purposes
certificate for import and export of wild animals and plants
certificate for inventor's patent right
certificate for land use
certificate for liquidation of debts
certificate for ownership of grassland
certificate for payment by mandate
certificate for permanent office of foreign news agency in China
certificate for protection of traditional Chinese medical species
certificate for qualifications in realty management
certificate for registration of special signs
certificate for release from reeducation through labor
certificate for release upon completion of a sentence
certificate for relief from compulsory abandonment of drug habits
certificate for the completion of a course of study
certificate for the ownership of mountain forest
certificate for the registration of computer software
certificate for the registration of contract for copyright authorization
certificate for the use of the place of business
certificate for transfer of foreign exchanges
certificate of accounts
certificate of acupuncture and moxibustion
certificate of addition
certificate of administrative protection of pharmaceuticals
certificate of airworthiness
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