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Database: 365,228(8 Aug 2026)

Drug Analysis Revision

Drug Analysis Revision, Total:60 items.

The international standard classification for "Drug Analysis Revision" includes: Protection against crime , General methods of tests and analysis for food products .

The Chinese standard classification for "Drug Analysis Revision" includes: Crime judging technology , Basic standards and general methods .


Professional Standard - Agriculture

  • 药典55-2014 Announcement on the addition and revision of the appendix Microbiology and Biological Testing of the Third Supplement to the 2010 Edition of the Chinese Pharmacopoeia
  • 225药典 第三增补本-2010 Appendix XIX F of the Revised Appendices of Part II Guidelines for the Analysis of Drug Impurities

Professional Standard - Public Safety Standards

  • GA/T 192-1998 Testing record contents and prescribed forms for toxicological analysis

Taiwan Provincial Standard of the People's Republic of China

未注明发布机构

Professional Standard - Nuclear Industry

  • EJ/T 839-1994 Standard format and content of radioactive material transport safety analysis report

国家质量监督检验检疫总局

  • SN/T 4747.1-2017 Determination of macrolide residues in live animal for import and export-Radio-receptor assay method
  • SN/T 4810-2017 Determination of β-lactams residues of live animals for import and export-Radio-receptor assay method

Professional Standard - Environmental Protection

  • HJ 168-2010 Environmental monitoring-Technical guideline on drawing and revising analytical method standards

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

  • GB/T 21174-2007 Determination of β-Lactams residues in animal derived food—Radio-receptor assay method

AIA/NAS - Aerospace Industries Association of America Inc.

  • NAS411-1-2016 HAZARDOUS MATERIALS TARGET LIST (Rev 1; Includes Access to Additional Content)

Association Francaise de Normalisation

  • NF EN ISO 5492/A1:2017 Analyse sensorielle - Vocabulaire - Amendement 1
  • NF X20-201*NF EN ISO 6141:2015 Gas analysis - Contents of certificates for calibration gas mixtures
  • NF ISO 6142-1/A1:2021 Gas analysis - Preparation of gas mixtures for calibration - Part 1: gravimetric method for Class I mixtures - Amendment 1: correction of the formulas in Annex E and Annex G

Standard Association of Australia (SAA)

AASHTO - American Association of State Highway and Transportation Officials

SCC

  • AWWA WQTC59003 Endocrine Disruptor & Pharmaceutical Analysis Using Direct-Injection LC/MS/MS
  • DANSK DS/EN ISO 6141:2015 Gas analysis - Contents of certificates for calibration gas mixtures
  • DANSK DS/EN ISO 6141/A1:2015 Gas analysis - Contents of certificates for calibration gas mixtures
  • ISO/IEC 15938-1:2002/AMD1:2005/COR1:2005 Corrigendum 1 - Amendment 1 - Information technology - Multimedia content description interface - Part 1: Systems - Systems extensions - Amendment 1 - Information technology - Multimedia content description interface - Part 1: Systems
  • ISO/IEC 15938-3:2002/AMD2:2006/COR1:2007 Corrigendum 1 - Amendment 2 - Information technology - Multimedia content description interface - Part 3: Visual - Perceptual 3D Shape Descriptor - Amendment 2 - Information technology - Multimedia content description interface - Part 3: Visual
  • AATCC 20-2007 Fiber Analysis: Qualitative (Editorial Revision 2009)
  • DIN EN ISO 11114-1/A1 E:2022 Draft Document - Gas cylinders - Compatibility of cylinder and valve materials with gas contents - Part 1: Metallic materials - Amendment 1 (ISO 11114-1:2020/DAM 1:2022); German and English version EN ISO 11114-1:2020/prA1:2022
  • NS-EN ISO 6141:2015 Gas analysis — Contents of certificates for calibration gas mixtures (ISO 6141:2015)
  • NS-EN 13503-5:2001 Ophthalmic implants — Intraocular lenses — Part 5: Biocompatibility (ISO 11979-5:1999, modified)
  • AWWA WQTC65970 Screening Analysis of Pharmaceutically Active Compounds in Water
  • AWWA WQTC64030 Analysis of Pharmaceutical Compound in Residual Water of a Hospital
  • BS 1676-6:1967 Containers for pharmaceutical dispensing. Specification for glass medicine bottles
  • DIN EN ISO 6141 E:2013 Draft Document - Gas analysis - Contents of certificates for calibration gas mixtures(ISO/DIS 6141:2013); German version prEN ISO 6141:2013

RU-GOST R

  • GOST R 53870-2010 Services on lower-limb prosthetics. Composition, contents and the order of rendering the services
  • GOST R 57105-2016 Integrated Logistic Support. Logistic Support Analysis. Requirements for Database Structure and Content

British Standards Institution (BSI)

ES-UNE

  • UNE-EN ISO 6141:2015 Gas analysis - Contents of certificates for calibration gas mixtures (ISO 6141:2015)

German Institute for Standardization

  • DIN EN ISO 6141:2020-05 Gas analysis - Contents of certificates for calibration gas mixtures (ISO 6141:2015 + Amd. 1:2020); German version EN ISO 6141:2015 + A1:2020
  • DIN EN ISO 6141:2020 Gas analysis - Contents of certificates for calibration gas mixtures (ISO 6141:2015 + Amd. 1:2020) (includes Amendment :2020)

GSO

  • GSO ISO 6141:2021 Gas analysis — Contents of certificates for calibration gas mixtures

US-CFR-file

  • CFR 21-316.20-2013 Food and drugs. Part316:Orphan drugs. Section316.20:Content and format of a request for orphan-drug designation.
  • CFR 21-316.26-2013 Food and drugs. Part316:Orphan drugs. Section316.26:Amendment to orphan-drug designation.

IN-BIS

  • IS 10280-1993 Earth-moving machinery. Operation and maintenance. Format and content of manuals (First Revision)

SG-SPRING SG

  • SS 152 AMD 1-2010 Identification of contents of industrial gas containers Amendment No.1

Institute of Interconnecting and Packaging Electronic Circuits (IPC)

ATIS - Alliance for Telecommunications Industry Solutions

  • 0410002-0029-2016 Unified Ordering Model (UOM) Volume II - Analysis For Access Service Ordering Guidelines (ASOG) (Version 54; Includes Access to Additional Content)

IX-EU/EC

  • (EU) 2015-152 Annex to Revision (EU) No 37/2010 for the pharmacologically active substance toramycin
  • (EU) 2015-394 Annex to Revision (EU) No 37/2010 for the pharmacologically active substance toramycin
  • (EU) 2015-150 Annex to Amendment (EU) No 37/2010 for the pharmacologically active substance gamithromycin
  • 1999/104/EC-1999 Amending the Annex to Council Directive 81/852/EEC on the Approximation of the Laws of the Member States Relating to Analytical, Pharmacotoxicological and Clinical Standards and Protocols in Respect of the Testing of Veterinary Medicinal Products
  • (EU) 2015-151 Annex to Amendment (EU) No 37/2010 for the pharmacologically active substance deoxyoxytetracycline
  • COM(2003) 29 FINAL-2003 COUNCIL DIRECTIVE amending Directive 78/660/EEC as regards amounts expressed in euro

International Organization for Standardization (ISO)

  • ISO/IEC 15938-3:2002/Amd 1:2004 Information technology — Multimedia content description interface — Part 3: Visual — Amendment 1: Visual extensions

Japanese Industrial Standards Committee (JISC)

Korean Agency for Technology and Standards (KATS)

KR-KS