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Drug Production Requirements

Drug Production Requirements, Total:12 items.

The international standard classification for "Drug Production Requirements" includes: Pharmaceutics .

The Chinese standard classification for "Drug Production Requirements" includes: Pharmaceutical processing machinery and equipment , Pharmaceutical, safety machinery and tool in general .


Group Standards of the People's Republic of China

  • T/ZAII 030-2021 Requirements for interconnection interface of GMP information system in pharmaceutical manufacturing enterprises
  • 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

Jiangsu Provincial Standard of the People's Republic of China

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

Professional Standard - Machinery

  • JB 20067-2005 General rule of pharmaceutical machinery conform to good anufacturing practice

Professional Standard - Military and Civilian Products

  • WJ 2404-1997 Ammunition charge assembly production safety requirements

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB 28670-2012 General rule of pharmaceutical machinery conforming to good manufacturing practice

RU-GOST R

  • 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

Korean Agency for Technology and Standards (KATS)

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

GOST

  • GOST R 52896-2007 Manufacturing of medicinal products. Processing equipment for manufacturing of solid dosage forms. General requirements