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Database: 365,228(8 Aug 2026)

South Pharmaceutical

South Pharmaceutical, Total:33 items.

The international standard classification for "South Pharmaceutical" includes: Plant growing .

The Chinese standard classification for "South Pharmaceutical" includes: Agriculture and forestry technology .


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

  • GB/T 32773-2016 Technical regulations of raw material forest for high-yielding Taxus wallichiana var.mairei paclitaxel

Professional Standard - Agriculture

Group Standards of the People's Republic of China

  • T/CIATCM 025-2019 Guidelines on construction of the quality management and control system for decocting Chinese medicine
  • T/CACM 001-2017 Guidelines for quality evaluation methods of traditional Chinese medicines
  • T/ZNX 001-2022 Intelligent Manufacturing Technology Guide for Pesticide Production
  • T/CACM 1607-2024 Technical guidelines for quality control of Chinese medicine manufacturing process
  • T/CACM 1606-2024 Technical guidelines for pharmaceutical process analytical technology of Chinese medicine
  • T/CAPDA 035-2022 Guideline for green pesticide formulations assessment
  • T/WSJD 56-2024 Guidelines for the Prevention and Control of Occupational Disease Hazards in the Pharmaceutical Industry
  • T/WSJD 60-2024 Guidelines for the Assessment and Control of Occupational Hazards of Active Pharmaceutical Ingredients in the Pharmaceutical Industry
  • T/CDAS 007-2022 Environmental Management Guidelines for Pharmaceutical Enterprises
  • T/CI 028-2023 General Principles for the Establishment of Foreign Introducing Traditional Chinese Medicine

Professional Standard - Environmental Protection

  • HJ 1256-2022 Self-monitoring technology guidelines for pollution sources ―Pharmaceutical industry Chinese traditional medicine category, biological pharmaceutical products category, chemical pharmaceutics preparations category

Compressed Gas Association (U.S.)

  • CGA M-11-2014 Guideline for compliance with the quality systems approach to pharmaceutical CGMPS

US-FCR

US-HHS

Korean Agency for Technology and Standards (KATS)

  • KS P 2080-2020 Guidelines for labelling to identify decocted herbal medicinal preparations

American Society for Testing and Materials (ASTM)

  • ASTM E2500-25 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment Science and Risk Based Approach
  • ASTM E2537-16(2024) Standard Guide for Application of Continuous Process Verification to Pharmaceutical and Biopharmaceutical Manufacturing
  • ASTM E2537-16 Standard Guide for Application of Continuous Process Verification to Pharmaceutical and Biopharmaceutical Manufacturing
  • ASTM E2500-20 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment

Association Francaise de Normalisation

  • XP CEN ISO/TS 23758:2021 Guidelines for the validation of qualitative methods for screening for veterinary drug residues in milk and dairy products