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中国药典1953年版颁布后,制药厂即按照药典规定对产品进行质量检验出厂,医药经营部门按规定验收、调拨,药政药检管理部门按规定进行监督管理,开始进入药品质量管理的法制化。由于药典附录注射剂通则项内的“注射液的澄明度”检查
After the promulgation of the Chinese Pharmacopoeia in 1953, the pharmaceutical factory manufactured the products according to the Pharmacopoeia. The pharmaceutical department under inspection and acceptance, transfer and administration of pharmaceutical and drug administration conducted supervision and management in accordance with the regulations and began to enter the legalization of pharmaceutical quality control. Due to the Pharmacopoeia Appendix Injection General items “clarity of the injection” check