食品及药物管理局宣布了针对人类血液和血液组分的采集，加工和存储的药品生产质量管理规范(GMP)。
The FDA declares Good Manufacturing Practices (GMP) for the collection, processing, and storage of human Blood and Blood components.
第三十二条临床研究用药物，应当在符合《药品生产质量管理规范》条件的车间制备。
Article 32 Drugs for use in clinical study shall be prepared in workshops meeting the conditions provided for in the Criterions for the Quality Control of Drug Manufacturing.
第三十二条临床研究用药物，应当在符合《药品生产质量管理规范》条件的车间制备。
Article 32 Drugs for use in clinical study shall be prepared in workshops meeting the conditions provided for in the Criterions for the Quality Control of Drug Manufacturing.
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