巴西药品生产GMP英文版
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2010年巴西ANVISA和卫生部公布RDC17 Dispõe sobre as Boas Práticas de Fabricação de Medicamentos， 规定了药品生产GMP的要求，采用了WHO Technical Report Series 908的要求。established the adoption of Report Nº 37 of
the WHO (WHO Technical Report Series 908), published in 2003.
如下是官方英文翻译全版和葡萄牙语版。
