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Database: 365,228(8 Aug 2026)

Medical verification

Medical verification, Total:64 items.

The international standard classification for "Medical verification" includes: Other standards related to freight distribution of goods , Pharmaceutics , Medical Sciences and health care facilities in general , Management of human resources .

The Chinese standard classification for "Medical verification" includes: Marking, packaging, transport and storage in general , Pharmaceutical, safety machinery and tool in general , Medical science , Legal medical expert .


Inner Mongolia Provincial Standard of the People's Republic of China

  • DB15/T 916-2015 Management specification for verification of pharmaceutical logistics facilities and equipment
  • DB15/T 963-2016 Medical logistics document management

Group Standards of the People's Republic of China

  • T/GZYJNY 05-2018 Agriculture of traditional Chinese medical science
  • T/CACM 1399-2022 Evidence-based practice guide for traditional Chinese medicine prevention and treatment of diabetic foot
  • T/CACM 1579-2024 Acceptance specification of prepared slices of Chinese crude drugs in medical institutions
  • T/CFLP 0013-2018 Temperature control validation of pharmaceutical refrigerated vehicles Specification for performance qualification
  • T/CACM 1335.2-2020 Standardized Operating Procedures for Overall Evidence Research of Traditional Chinese Medicine Part 2: Combing the Evidence from Ancient Books
  • T/SHQAP 004-2023 Medical laboratory equipment Fume hood

Professional Standard - Public Safety Standards

中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会

  • GB/T 34399-2017 Temperature control facilities of pharmaceutical products cold chain logistics - Specification for performance qualification

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

  • GB/T 28671-2012 Guidelines for pharmaceutical machinery validation
  • GB/T 51086-2015 Standard for terminology of pharmaceutical laboratory engineering
  • GB/T 27409-2010 Application of proficiency testing in the medical laboratory
  • GB 50457-2019 Code for design of pharmaceutical industry clean room

Professional Standard - Machinery

  • JB/T 20091-2007 Guidance on validation of pharmaceutical machinery(equipment)

Professional Standard - Agriculture

司法部

  • SF/T 0063-2020 General rules for method validation in forensic toxicology

Association Francaise de Normalisation

British Standards Institution (BSI)

  • BS EN 16679:2014 Packaging. Tamper verification features for medicinal product packaging
  • BS EN ISO 21976:2020 Packaging. Tamper verification features for medicinal product packaging
  • BS EN 1614:2006 Health informatics - Representation of dedicated kinds of property in laboratory medicine
  • BS ISO 21474-2:2022 In vitro diagnostic medical devices. Multiplex molecular testing for nucleic acids - Validation and verification

Spanish Association for Standardization (UNE)

  • UNE-EN 16679:2015 Packaging - Tamper verification features for medicinal product packaging
  • UNE-EN ISO 21976:2021 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)
  • UNE 171340:2020 Validation and qualification of controlled environments in hospitals

IT-UNI

European Committee for Standardization (CEN)

  • EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)
  • EN 1614:2006 Health informatics - Representation of dedicated kinds of property in laboratory medicine
  • prEN 13631-10-2021 Explosives for civil uses - Explosives - Part 10: Method for the verification of the means of initiation of explosives
  • EN 16679:2014 Packaging - Tamper verification features for medicinal product packaging

Danish Standards Foundation

  • DS/ISO 21976:2020 Packaging – Tamper verification features for medicinal product packaging
  • DS/EN ISO 21976:2020 Packaging – Tamper verification features for medicinal product packaging (ISO 21976:2018)

International Organization for Standardization (ISO)

  • ISO 21976:2018 Packaging — Tamper verification features for medicinal product packaging

SCC

  • DANSK DS/ISO 21976:2020 Packaging – Tamper verification features for medicinal product packaging
  • NS-EN 16679:2014 Packaging — Tamper verification features for medicinal product packaging
  • DANSK DS/EN 16679:2015 Packaging – Tamper verification features for medicinal product packaging
  • BS ISO 21976:2018 Packaging. Tamper verification features for medicinal product packaging
  • DIN EN 16679 E:2013 Draft Document - Packaging - Tamper verification features for medicinal product packaging; German version prEN 16679:2013
  • NS-EN ISO 21976:2020 Packaging — Tamper verification features for medicinal product packaging (ISO 21976:2018)
  • DANSK DS/EN ISO 21976:2020 Packaging – Tamper verification features for medicinal product packaging (ISO 21976:2018)
  • AAMI ST98:2022 Cleaning validation of health care products - Requirements for development and validation of a cleaning process for medical devices
  • DANSK DS/ISO 18665:2015 Traditional Chinese medicine – Herbal decoction apparatus

German Institute for Standardization

  • DIN EN ISO 21976:2020-12 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018); German version EN ISO 21976:2020
  • DIN EN ISO 21976 E:2020-07 Tamper verification functionality for packaged pharmaceutical product packaging (draft)
  • DIN EN 16679 E:2013-11 Packaging - Tamper verification features for medicinal product packaging
  • DIN EN 16679:2015 Packaging - Tamper verification features for medicinal product packaging; German version EN 16679:2014
  • DIN EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018); German version EN ISO 21976:2020

CH-SNV

  • SN EN ISO 21976:2021 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)

PL-PKN

Lithuanian Standards Office

  • LST EN ISO 21976:2020 Packaging - Tamper verification features for medicinal product packaging (ISO 21976:2018)

RU-GOST R

  • GOST R 52537-2006 Manufacturing of medicinal product. Quality assurance system. General requirements

American Society for Testing and Materials (ASTM)

  • ASTM E3051-16 Standard Guide for Specification, Design, Verification, and Application of Single-Use Systems in Pharmaceutical and Biopharmaceutical Manufacturing

ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc.

ET-QSAE

  • ES 543-2000 Non-aqueous titration of pharmaceuticals and medicinal products

Compressed Gas Association (U.S.)

  • CGA M-4-2012 VALIDATION OF MEDICAL CYLINDER FILLING SYSTEMS

SE-SIS

GSO

FI-SFS

US-CFR-file

  • CFR 21-316.21-2013 Food and drugs. Part316:Orphan drugs. Section316.21:Verification of orphan-drug status.

Military Standards (MIL-STD)