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pharmaceutical

pharmaceutical, Total:390 items.

In the international standard classification, pharmaceutical involves: Vocabularies, Pharmaceutics, Organic chemicals, Quality, HEALTH CARE TECHNOLOGY, Environmental protection, Seals, glands, Analytical chemistry, Measurement of volume, mass, density, viscosity, Pesticides and other agrochemicals, Petroleum products in general, Occupational safety. Industrial hygiene, Products of the chemical industry, Bottles. Pots. Jars, Lubricants, industrial oils and related products, Wastes, Air quality, Water quality, Glass, Reinforced plastics, Applications of information technology, Fertilizers, Medical equipment, Energy and heat transfer engineering in general, Industrial automation systems, Wood-based panels, Prepackaged and prepared foods, Information sciences. Publishing, Pipeline components and pipelines, Rubber and plastics products, Equipment for the chemical industry, Company organization and management, Processes in the food industry, Beekeeping, Aircraft and space vehicles in general, Packaging and distribution of goods in general, Equipment for children, Standardization. General rules.


American Society for Testing and Materials (ASTM), pharmaceutical

  • ASTM E2363-23 Standard Terminology Relating to Manufacturing of Pharmaceutical and Biopharmaceutical Products in the Pharmaceutical and Biopharmaceutical Industry
  • ASTM E2537-16 Standard Guide for Application of Continuous Process Verification to Pharmaceutical and Biopharmaceutical Manufacturing
  • ASTM E2500-07 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment
  • ASTM E2500-20 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment
  • ASTM E2500-13 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment
  • ASTM E1094-98(2003) Standard Specification for Pharmaceutical Glass Graduates
  • ASTM E1094-98 Standard Specification for Pharmaceutical Glass Graduates
  • ASTM E1094-04 Standard Specification for Pharmaceutical Glass Graduates
  • ASTM E3077-17 Standard Guide for Raw Material eData Transfer from Material Suppliers to Pharmaceutical & Biopharmaceutical Manufacturers
  • ASTM E3077-17e2 Standard Guide for Raw Material eData Transfer from Material Suppliers to Pharmaceutical & Biopharmaceutical Manufacturers
  • ASTM E1094-04(2009) Standard Specification for Pharmaceutical Glass Graduates
  • ASTM E1094-04(2015) Standard Specification for Pharmaceutical Glass Graduates
  • ASTM E2968-23 Standard Guide for Application of Continuous Manufacturing (CM) in the Pharmaceutical Industry
  • ASTM E2363-14 Standard Terminology Relating to Process Analytical Technology in the Pharmaceutical Industry
  • ASTM E2968-14 Standard Guide for Application of Continuous Processing in the Pharmaceutical Industry
  • ASTM E3326-22 Standard Guide for Application of Continuous Manufacturing (BioCM) in the Biopharmaceutical Industry
  • ASTM E2363-06a Standard Terminology Relating to Process Analytical Technology in the Pharmaceutical Industry
  • ASTM E2363-06 Standard Terminology Relating to Process Analytical Technology in the Pharmaceutical Industry
  • ASTM E1567-93(2001) Standard Guide for Biopharmaceutical Facilities Architectural Design Considerations
  • ASTM E1567-93 Standard Guide for Biopharmaceutical Facilities Architectural Design Considerations
  • ASTM E2474-06 Standard Practice for Pharmaceutical Process Design Utilizing Process Analytical Technology
  • ASTM E3051-16 Standard Guide for Specification, Design, Verification, and Application of Single-Use Systems in Pharmaceutical and Biopharmaceutical Manufacturing
  • ASTM E2891-13 Standard Guide for Multivariate Data Analysis in Pharmaceutical Development and Manufacturing Applications
  • ASTM E2474-14 Standard Practice for Pharmaceutical Process Design Utilizing Process Analytical Technology
  • ASTM E3077-17e1 Standard Guide for Raw Material eData Transfer from Material Suppliers to Pharmaceutical & Biopharmaceutical Manufacturers
  • ASTM E3230-20 Standard Practice for Extraction of Particulate Matter from the Surfaces of Single-Use Components and Assemblies Designed for Use in Biopharmaceutical Manufacturing
  • ASTM E3060-23 Standard Guide for Subvisible Particle Measurement in Biopharmaceutical Manufacturing Using Dynamic (Flow) Imaging Microscopy
  • ASTM E2656-10 Standard Practice for Real-time Release Testing of Pharmaceutical Water for the Total Organic Carbon Attribute
  • ASTM E3263-22 Standard Practice for Qualification of Visual Inspection of Pharmaceutical Manufacturing Equipment and Medical Devices for Residues
  • ASTM E2476-09 Standard Guide for Risk Assessment and Risk Control as it Impacts the Design, Development, and Operation of PAT Processes for Pharmaceutical Manufacture

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

  • GB/T 15692.6-1995 Water for pharmaceutical use
  • GB/T 15692.9-1995 Terms of pharmaceutical machinery--Other pharmaceutical machinery and equipment
  • GB/T 15692-2008 Terms of pharmaceutical machinery
  • GB/T 15692.3-1995 Terms of pharmaceutical machinery--Preparation machinery
  • GB/T 28671-2012 Guidelines for pharmaceutical machinery validation
  • GB/T 28258-2012 Classification and codes for pharmaceutical machinery products
  • GB/T 15692.1-1995 Terms of pharmaceutical machinery--General terms
  • GB/T 15692.5-1995 Terms of pharmaceutical machinery--Sliced herbal medicine machinery
  • GB/T 42354-2023 Pharmaceutical machinery (equipment) material selection guidelines
  • GB/T 15692.7-1995 Terms of pharmaceutical machinery--Pharmaceutical packaging machinery
  • GB/T 15692.8-1995 Terms of pharmaceutical machinery--Medicine detecting instrument
  • GB/T 15692.4-1995 Terms of pharmaceutical machinery--Pharmaceutical milling machinery
  • GB 37823-2019 Discharge Standards of Pollutants for Pesiticides Manufacture -----Sulfonylurea Family
  • GB/Z 42540-2023 Pharmaceutical Equipment Containment Technical Guidelines for Solid Preparations
  • GB/T 15692.2-1995 Terms of pharmaceutical machinery--Machinery and equipment for pharmaceutical material
  • GB/T 36036-2018 Verify guidance of cleaning and sterilization for pharmaceutical machinery
  • GB 21903-2008 Discharge standard of water pollutants for pharmaceutical industry Fermentation products category
  • GB 21905-2008 Discharge standard of water pollutants for pharmaceutical industry Extraction products category
  • GB 21908-2008 Discharge standard of water pollutants for pharmaceutical industry Mixing/Compounding and formulation category
  • GB/Z 42344-2023 Guidelines for Validation of Pharmaceutical Machinery (Equipment) Computerized System
  • GB 21904-2008 Discharge standard of water pollutants for pharmaceutical industry Chemical synthesis products category
  • GB 21907-2008 Discharge standard of water pollutants for pharmaceutical industry Bio-pharmaceutical category
  • GB/T 36035-2018/X1-2022 General Requirements for Electrical Safety of Pharmaceutical Machinery "No. 1 Amendment"
  • GB/T 36035-2018(XG1-2022) General Requirements for Electrical Safety of Pharmaceutical Machinery "No. 1 Amendment"
  • GB 28670-2012 General rule of pharmaceutical machinery conforming to good manufacturing practice
  • GB/T 32239-2015 Chinese medicine pill making machine

TH-TISI, pharmaceutical

  • TIS 2119-2013 Water for pharmaceutical purposes
  • TIS 640.1-2010 Ethanol for pharmaceutical use
  • TIS 1879-1999 Sodium chloride for pharmaceutical industry
  • TIS 939-1990 Standard for barium sulphate for pharmaceutical use
  • TIS 1212-1994 Turpentine for pharmaceutical industry
  • TIS 1211-1994 Acetaminophen for pharmaceutical use
  • TIS 1167-1993 Acetylsalicylic acid for pharmaceutical industry
  • TIS 847-2002 Magnesium hydroxide paste for pharmaceutical industry
  • TIS 2497-2010 Soft paraffin for pharmaceutical and cosmetic industries
  • TIS 508-2002 Aluminium hydroxide compressed gel for pharmaceutical industry
  • TIS 1247-2006 Liquid paraffin for pharmaceutical and cosmetic industries
  • TIS 509-1984 Standard for dried aluminium hydroxide gel for pharmaceutical industry
  • TIS 501-2003 Test methods for chemical resistance of pharmaceutical glass containers
  • TIS 889-1989 Standard for glass bottles for injection preparations and sterile pharmaceutical products nominal size not more than 300

RO-ASRO, pharmaceutical

  • STAS 12239-1984 SUGAR FOR PHARMACEUTICAL USE
  • STAS 3833-1981 THREADED GLASS JARS FOR CHEMICAL AND PHARMACEU- TICAL PRODUCTS
  • STAS SR 13356-1996 Enzyme preparations for food, pharmaceutical, textile-leather and detergent industry. Bacterial proteinase. Enzyme activity determination

US-HHS, pharmaceutical

US-FCR, pharmaceutical

ET-QSAE, pharmaceutical

CN-STDBOOK, pharmaceutical

  • 图书 3-9945 Pharmaceuticals for Parents and Relatives: Yangzijiang Pharmaceutical Quality Risk Control Model

Standard Association of Australia （SAA）, pharmaceutical

  • AS 1952:2009 Dispensing measures pharmaceutical glass
  • AS 1952:2009/Amdt 1:2012 Dispensing measures pharmaceutical glass
  • AS 1807.18:2000 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test - Determination of vibration in workstations, safety cabinets and pharmaceutical isolators
  • AS 1807.2:2000 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators Methods of test Determination of performance of clean workstations, laminar flow safety cabinets and pharmaceutical isolators under loaded filter conditions
  • AS 1807.1:2000 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test Determination of air velocity and uniformity of air velocity in clean workstations, laminar flow safety cabinets and pharmaceutical isolators
  • AS 1807.5:2000 Cleanrooms, workstations, safety cabinets and pharmaceutical isolators - Methods of test - Determination of work zone integrity

Professional Standard - Agriculture, pharmaceutical

Shanxi Provincial Standard of the People's Republic of China, pharmaceutical

  • DB14/T 2549-2022 Standards for management of traditional Chinese medicine laboratories for quality control in pharmaceutical companies
  • DB14/T 2547-2022 Pharmaceutical enterprise quality control chemical drug laboratory management specification
  • DB14/T 2548-2022 Quality Control Bioassay Laboratory Management Specifications for Pharmaceutical Enterprises

CZ-CSN, pharmaceutical

Professional Standard - Pharmaceutical Packaging, pharmaceutical

  • YBB 0004-2004 Medicinal vials made of borosilicate glass tubing
  • YBB 0005-2004 Medicinal bottles made of moulded borosilicate glass
  • YBB 0036-2003 Nagaiboli Guanzhi Yaoping Medicinal vials made of soda lime glass tubing
  • YBB 0030-2003 Dipengguiboli Mozhi Yao Ping
  • YBB 0035-2003 Dipengguiboli Guanzhi Yaoping Medicine vials made of low borosilicate glass tubing
  • YBB 0036(03)-2003 Soda-lime glass controlled pharmaceutical bottle (trial)
  • YBB 0030(03)-2003 Low borosilicate glass molded pharmaceutical bottle (trial)
  • YBB 0035(03)-2003 Low borosilicate glass controlled pharmaceutical bottles (trial)

IN-BIS, pharmaceutical

  • IS 3692-1975 Specification for rubber bottle caps for pharmaceuticals
  • IS 10627-1983 Sampling methods for pesticide preparations

Professional Standard - Medicine, pharmaceutical

  • YY/T 0192-1994 Standard system table for pharmaceutical machinery
  • YY/T 0216-1995 Editorial nominating method for the model designation of pharmaceutical machinery
  • YY 0260-1997 Classification and codes for pharmaceutical machinery products

HU-MSZT, pharmaceutical

  • MNOSZ 9555-1953 Salicylic acid for the pharmaceutical industry and industry

CU-NC, pharmaceutical

  • NC 26-211-1992 Good Manufacturing Practices For Pharmaceutical Products
  • NC 26-160-1986 Veterinary Drugs. Mammary Infusions. General Quality Specifications
  • NC 26-181-1987 Pharmaceutical Industry Defatted Páncreas Powder Quality Specifications

工业和信息化部/国家能源局, pharmaceutical

Professional Standard - Machinery, pharmaceutical

Group Standards of the People's Republic of China, pharmaceutical

  • T/CDAS 007-2022 Environmental Management Guidelines for Pharmaceutical Enterprises
  • T/ZZB 0668-2018 Sanitary mechanical seals for food and pharmaceutical industries
  • T/APEP 1026-2022 Discharge Standards for Water Pollutants of Traditional Chinese Medicine Pharmaceutical Industry
  • T/CAB 2009-2017 Production of antibiotic-free mutton sheep and mutton quality requirements
  • T/ZAII 019-2019 Specification for informatization integration of pharmaceutical production quality control
  • T/ZAII 018-2019 Function framework for integrated management and control of pharmaceutical production
  • T/CAPEB 00001.2-2022 Pharmaceutical Equipment Containers and Piping Part 2: Materials
  • T/APEP 1022-2022 Discharge Standards for Water Pollutants in Fermentation Pharmaceutical Industry
  • T/APEP 1025-2022 Discharge Standards for Water Pollutants of Extracted Pharmaceutical Industry
  • T/CAPEB 00001.4-2022 Pharmaceutical Equipment Containers and Piping Part 4: Fittings
  • T/CAPEB 00001.8-2022 Pharmaceutical Equipment Containers and Piping Part 8: Validation
  • T/CAPEB 00001.3-2022 Pharmaceutical Equipment Vessels and Piping Part 3: Design
  • T/CAPEB 00001.7-2022 Pharmaceutical Equipment Containers and Piping Part 7: Inspection
  • T/APEP 1023-2022 Discharge Standards for Water Pollutants in Pharmaceutical Industry of Mixed Preparations
  • T/IMAS 070-2024 Organic fertilizers produced by biopharmaceutical intermediate by-products
  • T/CAPEB 00001.6-2022 Containers and piping for pharmaceutical equipment - Part 6: Fabrication and installation
  • T/APEP 1021-2022 Discharge Standards for Water Pollutants in Chemical Synthesis Pharmaceutical Industry
  • T/APEP 1024-2022 Discharge Standards for Water Pollutants in Bioengineering Pharmaceutical Industry
  • T/CAPEB 00001.5-2022 Pharmaceutical Equipment Containers and Piping Part 5: Piping Connections
  • T/CAPEB 00001.1-2022 Containers and piping for pharmaceutical equipment Part 1: General requirements
  • T/ZJPA 001-2021 Technical consideration of environmental microbial database construction in pharmaceutical industry
  • T/CASME 320-2023 Intelligent mobile workbenchwith high protection in pharnmaceutical industry
  • T/AHFIA 086-2023 Pre-made Vegetable Herbal Chicken with Pepper
  • T/AHFIA 087-2023 Prepared Vegetable Herbal Diet Peony Chicken
  • T/AHFIA 085-2023 Pre-made Vegetables Herbal Diet Ginseng Beef
  • T/PIAC 00004-2021 Technical Guidelines for Development of Chemicals Emission Scenario Documents in the Pharmaceutical Industry
  • T/SHBX 003-2023 Guideline for extractables testing of polymeric single-use components used in pharmaceutical manufacturing
  • T/ZGM 004-2022 Assessment requirements for quality grading and forerunner - Microporous membrane elements for sterilization in the pharmaceutical industry
  • T/HNYJNYXH 005-2020 Standard of high-quality rice vinegar for processing traditional Chinese medicine
  • T/HNYJNYXH 004-2020 Standards for high-quality rice wine specially processed for traditional Chinese medicine
  • T/HNYJNYXH 007-2021 High-quality processed traditional Chinese medicine special honey standard
  • T/SDNY 001-2018 Limits of non-declared pesticide ingredients in pesticide preparations
  • T/IMAS 071-2024 Technical specification for safety risk assessment of organic fertilizer production by biopharmaceutical intermediate by-products

ISA - International Society of Automation, pharmaceutical

British Standards Institution (BSI), pharmaceutical

  • BS 1922:1987+A2:2011 Specification for glass dispensing measures for pharmaceutical purposes
  • BS ISO 11418-4:2006 Containers and accessories for pharmaceutical preparations - Tablet glass bottles
  • BS PD CEN/TR 17612:2021 Algae and algae products. Specifications for pharmaceutical sector applications
  • BS EN ISO 8871-2:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Identification and characterization
  • BS EN ISO 8871-5:2014 Elastomeric parts for parenterals and for devices for pharmaceutical use. Functional requirements and testing
  • BS 1000[615]:1979 Universal Decimal Classification - English full edition - Pharmaceutics - Therapeutics - Toxicology
  • BS EN ISO 8871-3:2004 Elastomeric parts for parenterals and for devices for pharmaceuticals use - Determination of released-particle count
  • BS EN ISO 8871-1:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Extractables in aqueous autoclavates
  • BS EN ISO 8871-3:2004+A1:2019 Elastomeric parts for parenterals and for devices for pharmaceutical use. Determination of released-particle count
  • BS EN ISO 8871-4:2006 Elastomeric parts for parenterals and for devices for pharmaceutical use - Biological requirements and test methods
  • BS CWA 15914-1:2009 Criteria, methodology and procedures for creating an E-codification concerning substances used in pharmaceutical compounding

Association Francaise de Normalisation, pharmaceutical

  • NF U43-215:1981 Agropharmaceutical products. Petroleum oils for the manufacture of agropharmaceutical products. Distillation.
  • FD CEN/TR 17612:2021 Algues et produits d'algues - Spécifications pour les applications dans le secteur pharmaceutique
  • NF H35-037:1987 Industries de l'embouteillage - Bague à vis plastique type "pharmacie" - Dimensions.
  • NF U43-216:1981 Agropharmaceutical products. Petroleum oils for the manufacture of agropharmaceutical products. Determination of non-sulphonated residue.
  • NF U43-214:1990 Agropharmaceutical products. Heavy oils for the manufacture of agropharmaceutical products. Specifications.
  • NF S93-102-2:2005 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2 : identification and characterization.
  • NF S93-102-5:2014 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5 : functional requirements and testing
  • NF S93-102-1*NF EN ISO 8871-1:2005 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 1 : Extractables in aqueous autoclavates
  • NF S93-102-2/A1:2014 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2 : identification and characterization - Amendment 1
  • NF S93-102-3*NF EN ISO 8871-3:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3 : determination of released-particule count
  • NF S93-102-4*NF EN ISO 8871-4:2006 Elastomeric parts for parenteral and for devices for pharmaceutical use - Part 4 : biological requirements and test methods
  • NF EN 16821:2017 Tuyaux et flexibles en caoutchouc et en plastique pour utilisation dans les industries pharmaceutique et biotechnologique - Tuyaux en silicone

Professional Standard-Safe Production, pharmaceutical

  • AQ/T 4255-2015 Specification for prevention and control of occupational detriment in pharmaceutical enterprises

Defense Logistics Agency, pharmaceutical

PL-PKN, pharmaceutical

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, pharmaceutical

  • GB/T 36035-2018 Pharmaceutical machinery—General requirements for electrical safety
  • GB/T 36030-2018 General technical requirements of CIP and SIP for pharmaceutical machinery

工业和信息化部, pharmaceutical

  • JB/T 20206-2022 Biopharmaceutical reaction process temperature control device
  • HG/T 5902-2021 Green factory evaluation requirements for the chemical and pharmaceutical industry

中华人民共和国环境保护部, pharmaceutical

  • 公告 2012年 第18号 Technical policy for pollution prevention and control in the pharmaceutical industry
  • GB 21906-2008 Discharge standard of water pollutants for pharmaceutical industry Chinese traditional medicine category

International Organization for Standardization (ISO), pharmaceutical

  • ISO/CD 12370 Guidelines for treatment and reuse of fermentation-based pharmaceutical wastewater
  • ISO/DIS 12370:2023 Guidelines for treatment and reuse of fermentation-based pharmaceutical wastewater
  • ISO 8871-2:2003 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization
  • ISO 8871-5:2005 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing
  • ISO 8871-5:2016 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing
  • ISO 8871-1:2003 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 1: Extractables in aqueous autoclavates
  • ISO 8871-3:2003 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count
  • ISO 8871-2:2003/Amd 1:2005 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization; Amendment 1
  • ISO 8871-4:2006 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods
  • ISO/TR 23975:2019 Traditional Chinese medicine — Priority list of single herbal medicines for developing standards

Anhui Provincial Standard of the People's Republic of China, pharmaceutical

  • DB34/ 310005-2021 Emission Standards of Air Pollutants for the Pharmaceutical Industry
  • DB34/T 4230.10-2022 Technical Specifications for Environmental Management of Volatile Organic Compounds in Key Industries Part 10: Pharmaceutical Industry

Zhejiang Provincial Standard of the People's Republic of China, pharmaceutical

  • DB33/ 310005-2021 Emission Standards of Air Pollutants for the Pharmaceutical Industry
  • DB33/ 923-2014 Pollutant Discharge Standards for Biopharmaceutical Industry

Jiangsu Provincial Standard of the People's Republic of China, pharmaceutical

  • DB32/ 4042-2021 Emission Standards of Air Pollutants for the Pharmaceutical Industry
  • DB32/ 3560-2019 Discharge limits of water and air pollutants in the biopharmaceutical industry

Shanghai Provincial Standard of the People's Republic of China, pharmaceutical

  • DB31/ 310005-2021 Emission Standards of Air Pollutants for the Pharmaceutical Industry
  • DB31/ 373-2010 Pollutant Discharge Standards for the Biopharmaceutical Industry

Yunnan Provincial Standard of the People's Republic of China, pharmaceutical

  • DB5301/T 52-2021 Discharge limits of water pollutants in traditional Chinese medicine pharmaceutical industry

Professional Standard - Environmental Protection, pharmaceutical

  • HJ 858.1-2017 Technical Specification for Application and Issuance of Pollutant Permit Pharmacy Industry—Active Pharmaceutical Ingredient Manufacturing
  • HJ 992-2018 Pollution Source Intensity Accounting Technical Guidelines for the Pharmaceutical Industry
  • HJ 611-2011 Technical guidelines for environmental impact assessment.Pharmaceutical constructional project
  • HJ 1062-2019 Pollutant Discharge Permit Application and Issuance Technical Specifications Pharmaceutical Industry-Biological Pharmaceutical Products Manufacturing
  • HJ 1063-2019 Pollutant Discharge Permit Application and Issuance Technical Specifications Pharmaceutical Industry-Manufacturing of Chemical Preparations
  • HJ 2044-2014 Technical specifications of wastewater treatment for fermentative pharmaceutical industry
  • HJ 792-2016 Technical guidelines for environmental protection in pharmaceutical constructional project for check and accept of completed construction project
  • HJ 881-2017 Technical guidelines for self-monitoring of sewage units Extraction pharmaceutical industry
  • HJ 882-2017 Technical guidelines for self-monitoring of pollutant discharge units Fermentation pharmaceutical industry
  • HJ 1064-2019 Application and issuance of pollutant discharge permits Technical Specifications Pharmaceutical Industry-Production of Chinese Proprietary Medicines
  • HJ 883-2017 Technical guidelines for self-monitoring of sewage units Chemical synthesis pharmaceutical industry
  • HJ 1256-2022 Technical guidelines for self-monitoring of pollutant discharge units

RU-GOST R, pharmaceutical

  • GOST R 57146-2016 Medicines for medical applications. Studying for carcinogenicity of pharmaceuticals and excipients
  • GOST R 51314-1999 Aluminium caps and caps made of aluminium-plastics combinations for medicine remedies. General specifications

国家市场监督管理总局、中国国家标准化管理委员会, pharmaceutical

Liaoning Provincial Standard of the People's Republic of China, pharmaceutical

  • DB21/T 2521-2015 Chemical Synthesis Pharmaceutical Safety Production Technical Regulations

Compressed Gas Association (U.S.), pharmaceutical

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

IT-UNI, pharmaceutical

  • UNI 6255-1968 Forged glass vials for pharmaceutical use. Dimensions and deviations
  • UNI 7530-1976 Technology, pharmaceutical and sanitary glass products. Determination of chlorine in hydrolysis transfer
  • UNI 7425-1975 Technology, pharmaceutical and sanitary glass products. Determination of iron in hydrolysis transfer
  • UNI 7528-1976 Technology, pharmaceutical and sanitary glass products. Determination of magnesium in hydrolysis transfer
  • UNI 7529-1976 Technology, pharmaceutical and sanitary glass products. Determination of lead in hydrolysis transfer
  • UNI 7221-1973 Technology, pharmaceutical and sanitary glass products. Determination of boron in hydrolysis transfer
  • UNI 7222-1973 Technology, pharmaceutical and sanitary glass products. Calcium determination in hydrolysis transfer
  • UNI 7403-1975 Technology, pharmaceutical and sanitary glass products. Chemical strength of glassy enamel
  • UNI 7220-1973 Technology, pharmaceutical and sanitary glass products. Determination of residual tension in glass products
  • UNI 6788-1971 Technology, pharmaceutical and sanitary glass products. Light guide measurement of glass containers in the 290-f-550nm spectral region

U.S. Military Regulations and Norms, pharmaceutical

AT-ON, pharmaceutical

Danish Standards Foundation, pharmaceutical

  • DS/CEN/TR 17612:2021 Algae and algae products – Specifications for pharmaceutical sector applications
  • DS/EN ISO 8871-3:2005 Elastomeric parts for parenterals and for devices for pharmaceuticals use - Part 3: Determination of released-particle count

European Committee for Standardization (CEN), pharmaceutical

  • PD CEN/TR 17612:2021 Algae and algae products - Specifications for pharmaceutical sector applications
  • EN ISO 8871-2:2020 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)
  • EN ISO 8871-5:2014 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2005)
  • EN ISO 8871-5:2016 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing
  • EN ISO 8871-3:2004 Elastomeric parts for parenterals and for devices for pharmaceuticals use - Part 3: Determination of released-particle count
  • EN ISO 8871-2:2004/A1:2014 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - Amendment 1 (ISO 8871-2:2003/Amd 1:2005)

ES-UNE, pharmaceutical

YU-JUS, pharmaceutical

  • JUS B.E4.201-1992 Glass containers for pharmaceutical and medical use.General technical
  • JUS B.E8.125-1988 Glass for laboratory and pharmaceutical use. Ejdrolitic resistance of the interior surfaces of glass containers. Hethods of test and classiflcation
  • JUS B.B6.034-1990 Calcium carbonate fillers. Naturaj calcium carbooate - grivding for use in pharma and cosmetica industry. Tecbnical requireaients

German Institute for Standardization, pharmaceutical

  • DIN 11854:2015-09 Components for the food and pharmaceutical industry - Hose unions of stainless steel
  • DIN 11850:1999 Tubes for the food, chemical and pharmaceutical industry - Stainless steel tubes - Dimensions, materials
  • DIN 11866:2016 Stainless steel components for aseptic applications in the chemical and pharmaceutical industry - Tubes
  • DIN 11866:2016-11 Stainless steel components for aseptic applications in the chemical and pharmaceutical industry - Tubes / Note: Applies in conjunction with DIN EN 10088-1 (2014-12), DIN EN 10216-5 (2014-03), DIN EN 10217-7 (2015-01).
  • DIN EN ISO 8871-2:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003); German version EN ISO 8871-2:2004, text in German and English
  • PAS 1050-1-2005 Guideline for the implementation of the TA Luft in the chemical and pharmaceutical industry-Part 1:General requirements
  • DIN 11864-1:2017 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Part 1: Connections
  • DIN ISO 8871-5:2006 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2005), text in German and English
  • DIN 11867:2012 Elbows for pigging systems, welding fittings in stainless steel, for aseptic, chemical and pharmaceutical industries
  • DIN 11867:2005 Elbows for pigging systems, welding fittings in stainless steel, for aseptic, chemical and pharmaceutical industries
  • DIN EN ISO 8871-1:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 1: Extractables in aqueous autoclavates (ISO 8871-1:2003); German version EN ISO 8871-1:2004, text in German and English
  • DIN 11867:2021 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Elbows for pigging systems
  • DIN EN ISO 8871-3:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count (ISO 8871-3:2003); German version EN ISO 8871-3:2004, text german and english
  • DIN 11867:2021-08 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Elbows for pigging systems
  • DIN 11864-1:2017-10 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Part 1: Connections
  • PAS 1050-2-2005 Guideline for the implementation of the TA Luft in the chemical and pharmaceutical industry-Part 2:Flanges and seals
  • DIN 32676:2009 Fittings for the food, chemical and pharmaceutical industries - Clamp connections for stainless steel tubes - Weld-on type
  • DIN EN ISO 8871-4:2006 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods (ISO 8871-4:2006); English version of DIN EN ISO 8871-4:2006-09
  • DIN 11864-2:2021 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Part 2: Flange connections
  • DIN 11865:2020 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Tees, elbows and reducers
  • DIN 11864-2:2023-08 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Part 2: Flange connections / Note: Date of issue 2023-07-21*Intended as replacement for DIN 11864-2 (2021-06).
  • DIN 11864-2:2021-06 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Part 2: Flange connections
  • DIN 11865:2020-07 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Tees, elbows and reducers
  • DIN 11864-3:2021-06 Stainless steel components for aseptic applications in the chemical and the pharmaceutical industries - Part 3: Clamp connections
  • DIN EN ISO 8871-2:2020 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)
  • DIN EN 14375 Berichtigung 1:2006 Child-resistant non-reclosable packaging for pharmaceutical products - Requirements and testing; German version EN 14375:2003, Corrigenda to DIN EN 14375:2004-02; German version EN 14375:2003/AC:2006

国家发展和改革委员会, pharmaceutical

  • JB/T 20067-2005 Pharmaceutical machinery complies with the General Principles of Good Manufacturing Practice for Pharmaceutical Products

Guangxi Provincial Standard of the People's Republic of China, pharmaceutical

  • DB45/T 724-2011 Equipment and management requirements for energy measuring instruments in the pharmaceutical industry

Henan Provincial Standard of the People's Republic of China, pharmaceutical

  • DB41/ 758-2012 Indirect Discharge Standards for Water Pollutants in Fermentation Pharmaceutical Industry
  • DB41/ 756-2012 Indirect Discharge Standards for Water Pollutants in Chemical Synthesis Pharmaceutical Industry

未注明发布机构, pharmaceutical

  • DIN EN ISO 8362-5:2014 Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use
  • DIN 11850 Tubes for the food, chemical and pharmaceutical industry - Stainless steel tubes - Dimensions, materials
  • DIN EN ISO 8871-2 E:2019-03 Elastomeric parts for parenteral and pharmaceutical devices Part 2: Identification and characterization (draft)
  • DIN 11867 E:2020-12 Elbows for pigging systems, welding fittings in stainless steel, for aseptic, chemical and pharmaceutical industries
  • DIN EN ISO 8871-5 E:2014-03 Elastomeric parts for parenteral and pharmaceutical devices Part 5: Functional requirements and testing (draft)
  • DIN EN ISO 8871-5 E:2015-08 Elastomeric parts for parenteral and pharmaceutical devices Part 5: Functional requirements and testing (draft)

United States Navy, pharmaceutical

Military Standards (MIL-STD), pharmaceutical

  • DOD A-A-51636 A-1987 SYRINGE, FLUID DISPENSING, 10 ML (PHARMACEUTICAL) [Use In Lieu Of: DOD A-A-0051636]

Korean Agency for Technology and Standards (KATS), pharmaceutical

  • KS J 0017-2010(2021) Quality system policy in biopharmaceutical production based on Good Manufacturing Practice
  • KS J 0015-2010(2021) Quality manual in biopharmaceutical production based on current Good Manufacturing Practice
  • KS J 0020-2010(2021) Production system policy in biopharmaceutical production based on Good Manufacturing Practice
  • KS J 0022-2010(2021) Laboratory control system policy in biopharmaceutical production based on Good Manufacturing Practice
  • KS P ISO 8871-2:2010 Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
  • KS J 0018-2010(2021) Materials system policy in biopharmaceutical production based on Good Manufacturing Practice
  • KS P ISO 8871-2:2017 Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 2：Identification and characterization
  • KS P ISO 8871-5:2010 Elastomeric parts for parenterals and for devices for pharmaceutical use-Part 5:Functional requirements and testing
  • KS J 0021-2010(2021) Packaging and labelling system policy in biopharmaceutical production based on Good Manufacturing Practice
  • KS J 0016-2010(2021) Facility and equipment system policy in biopharmaceutical production based on Good Manufacturing Practice
  • KS P ISO 8871-3:2009 Elastomeric parts for parenterals and for devices for pharmaceutical use-Part 3:Determination of released-particle count
  • KS P ISO 8871-5:2021 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 5: Functional requirements and testing
  • KS P ISO 8871-5-2010(2016) Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 5：Functional requirements and testing
  • KS P ISO 8871-4:2010 Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 4：Biological requirements and test methods
  • KS P ISO 8871-1-2010(2016) Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 1：Extractables in aqueous autoclavates
  • KS P ISO 8871-1:2010 Elastomeric parts for parenterals and for devices for pharmaceutical use-Part 1:Extractables in aqueous autoclavates
  • KS P ISO 8871-4-2010(2016) Elastomeric parts for parenterals and for devices for pharmaceutical use－Part 4：Biological requirements and test methods
  • KS P ISO 8871-4:2021 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 4: Biological requirements and test methods

IX-EU/EC, pharmaceutical

  • 85/434/EEC-1985 Council Decision Setting up an Advisory Committee on Pharmaceutical Training

KR-KS, pharmaceutical

  • KS P ISO 8871-2-2022 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 2: Identification and characterization
  • KS P ISO 8871-5-2021 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 5: Functional requirements and testing
  • KS P ISO 8871-4-2021 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 4: Biological requirements and test methods

Professional Standard - Certification and Accreditation, pharmaceutical

  • RB/T 114-2014 Energy management system.Certification requirements for chemical plants manufacturing sodium carbonate, coking, rubber and plastic products and pharmaceuticals
  • RB/T 114-2023 Energy management system certification requirements for chemical enterprises such as soda ash, coking, rubber and plastic products, and pharmaceuticals

Hebei Provincial Standard of the People's Republic of China, pharmaceutical

  • DB13/ 2208-2015 Penicillin Pharmaceutical Volatile Organic Compounds and Odor Characteristic Pollutants Emission Standards
  • DB13/T 5363-2021 Technical Guidelines for the Control of Volatile Organic Compounds and Odor Gas Pollution in Biological and Chemical Pharmaceutical Industries

U.S. Environmental Protection Agency (U.S. EPA), pharmaceutical

GB-REG, pharmaceutical

Association of German Mechanical Engineers, pharmaceutical

  • VDI 2083 Blatt 13.3-2010 Cleanroom technology - Quality, production, and distribution of ultrapure water - Pharmacy and other life-science applications

Lithuanian Standards Office , pharmaceutical

  • LST EN ISO 8871-2:2004 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003)

CH-SNV, pharmaceutical

  • SN EN ISO 8871-2:2020 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)

AENOR, pharmaceutical

  • UNE-EN ISO 8871-2:2005 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003)

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