CFDA: certification notice of quality management standard for non clinical drug research (No.4)
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Last Update: 2016-12-30
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Source: Internet
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Author: User
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Source: CFDA 2016-12-30 in accordance with the relevant provisions of the drug administration law of the people's Republic of China, the drug non clinical research quality management specification (drug GLP) and the drug non clinical research quality management specification certification management measures, the State Food and Drug Administration organized relevant experts to Suzhou Huace Biotechnology Co., Ltd Inspection was carried out by institutions According to the audit, the single and multiple dose toxicity tests (rodents) and other test items of the 8 institutions meet the requirements of GLP (see the annex) It is hereby announced Annex: drug GLP certification catalogue annex.docx of Announcement No 198 of the food and Drug Administration of the people's Republic of China on December 26, 2016
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