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Drug Production Requirements

Drug Production Requirements, Total:10 items.

In the international standard classification, Drug Production Requirements involves: Quality, Air quality, Pharmaceutics, Water quality, Interface and interconnection equipment.

Korean Agency for Technology and Standards (KATS), Drug Production Requirements

• KS J 0015-2010 Quality manual in biopharmaceutical production based on current Good Manufacturing Practice

RU-GOST R, Drug Production Requirements

• GOST R 52537-2006 Manufacturing of medicinal product. Quality assurance system. General requirements
• GOST R 52896-2017 Manufacturing of medicinal product. Manufacturing systems and equipment for the production of medicines. General requirements

Group Standards of the People's Republic of China, Drug Production Requirements

• T/SHPPA 010-2021 Technical requirements for digital quality assurance in pharmaceutical manufacturing
• T/SHQAP 002-2023 Technical requirements of digital traceability in the whole process of drug production——Manufacturing management
• T/CATCM 007-2019 Traditional Chinese Medicine Traceability Information Requirements for the Production of Chinese Herbal Pieces
• T/ZAII 030-2021 Requirements for interconnection interface of GMP information system in pharmaceutical manufacturing enterprises

Jiangsu Provincial Standard of the People's Republic of China, Drug Production Requirements

• DB32/T 3770-2020 Quality risk management and control system requirements for pharmaceutical manufacturing enterprises

Professional Standard - Military and Civilian Products, Drug Production Requirements

• WJ 2404-1997 Ammunition charge assembly production safety requirements

Beijing Provincial Standard of the People's Republic of China, Drug Production Requirements

• DB11/ 519-2008 Hygiene Requirements for Eating Raw Aquatic Products

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