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Treatment + Biological Products + Products

Treatment + Biological Products + Products, Total:499 items.

In the international standard classification, Treatment + Biological Products + Products involves: Biology. Botany. Zoology, Vocabularies, Wood, sawlogs and sawn timber, Dentistry, Laboratory medicine, Products of the chemical industry, Food products in general, Microbiology, Veterinary medicine, Quality, Meat, meat products and other animal produce, Information sciences. Publishing, Medical sciences and health care facilities in general, Services, Medical equipment, Bottles. Pots. Jars, Fuels, Wood technology processes, Sterilization and disinfection, Pharmaceutics, Soil quality. Pedology, Farming and forestry, Company organization and management, Products of the textile industry, Protection against dangerous goods, Fertilizers, Cereals, pulses and derived products, Leisure. Tourism, Air quality, Applications of information technology, Occupational safety. Industrial hygiene, Processes in the food industry, Construction industry, Radiation protection, Milk and milk products, Pesticides and other agrochemicals, Refractories, Wastes, Plastics, Freight distribution of goods, Rubber, Rubber and plastics products, Construction materials, General methods of tests and analysis for food products, Materials and articles in contact with foodstuffs.


Professional Standard - Agriculture, Treatment + Biological Products + Products

International Organization for Standardization (ISO), Treatment + Biological Products + Products

  • ISO 20399:2022 Biotechnology — Ancillary materials present during the production of cellular therapeutic products and gene therapy products
  • ISO/TS 23565:2021 Biotechnology — Bioprocessing — General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
  • ISO 21973:2020 Biotechnology — General requirements for transportation of cells for therapeutic use
  • ISO/TS 22456:2021 Sterilization of healthcare products - Microbiological methods - Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products
  • ISO/TS 20399-1:2018 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 1: General requirements
  • ISO 20404:2023 Biotechnology — Bioprocessing — General requirements for the design of packaging to contain cells for therapeutic use
  • ISO 10993-12:2002 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • ISO 10993-12:2021 Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
  • ISO 10993-12:2012 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • ISO 16954:2015 Dentistry - Test methods for dental unit waterline biofilm treatment
  • ISO 23033:2021 Biotechnology — Analytical methods — General requirements and considerations for the testing and characterization of cellular therapeutic products
  • ISO 10993-12:1996 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • ISO 10993-12:2007 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • ISO 11138-3:1995 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization
  • ISO/TS 20399-3:2018 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 3: Best practice guidance for ancillary material users
  • ISO/TS 20399-2:2018 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 2: Best practice guidance for ancillary material suppliers
  • ISO 11138-1:1994 Sterilization of health care products - Biological indicators - Part 1: General
  • ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • ISO 11138-2:1994 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization
  • ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • ISO 11138-1:2006 Sterilization of health care products - Biological indicators - Part 1: General requirements
  • ISO 11138-2:2006 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes
  • ISO 11737-1:2006 Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products
  • ISO 11737-1:1995 Sterilization of medical devices - Microbiological methods - Part 1: Estimation of population of microorganisms on products
  • ISO/TR 24290:2023 Health informatics — Datasets and data structure for clinical and biological evaluation metrics in radiotherapy
  • ISO 11138-2:2017 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes
  • ISO/DTR 24290 Health informatics — Datasets and data structure for clinical and biological evaluation metrics in radiotherapy
  • ISO/TR 24422:2022 Development of a water equivalent phantom to measure the physical characteristics of specific radiosurgery treatment devices
  • ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • ISO 10993-8:2000 Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests
  • ISO 11138-1:2017 Sterilization of health care products - Biological indicators - Part 1: General requirements
  • ISO 11737-1:2006/Cor 1:2007 Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products; Technical Corrigendum 1
  • ISO 6887-3:2017/Amd 1:2020 Microbiology of the food chain — Preparation of test samples, initial suspension and decimal dilutions for microbiological examination — Part 3: Specific rules for the preparation of fish and fishery
  • ISO 11138-5:2017 Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes
  • ISO 14161:2009 Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results
  • ISO 14161:2000 Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results
  • ISO 22442-2:2007 Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling

British Standards Institution (BSI), Treatment + Biological Products + Products

  • BS ISO 20399:2022 Biotechnology. Ancillary materials present during the production of cellular therapeutic products and gene therapy products
  • 22/30424231 DC BS ISO 20399. Biotechnology. Ancillary materials present during the production of cellular therapeutic products and gene therapy products
  • PD CEN/TS 15003:2005 Durability of wood and wood-based products - Criteria for hot air processes for curative uses against wood destroying organisms
  • BS EN ISO 10993-12:2004 Biological evaluation of medical devices - Sample preparation and reference materials
  • BS ISO 20404:2023 Biotechnology. Bioprocessing. General requirements for the design of packaging to contain cells for therapeutic use
  • BS EN 14128:2004 Durability of wood and wood-based products - Performance criteria for products for curative uses against wood attacking organisms as determined by biological tests
  • BS PD ISO/TS 22456:2021 Sterilization of healthcare products. Microbiological methods. Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products
  • BS ISO 21973:2020 Biotechnology. General requirements for transportation of cells for therapeutic use
  • PD ISO/TS 23565:2021 Biotechnology. Bioprocessing. General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
  • 22/30428167 DC BS ISO 20404. Biotechnology. Bioprocessing. General requirements for the design of packaging to contain cells for therapeutic use
  • BS EN 14128:2020 Tracked Changes. Durability of wood and wood-based products. Efficacy criteria for curative wood preservatives as determined by biological tests
  • 20/30369896 DC BS ISO 23033. Biotechnology. Analytical methods. General guidelines for the characterization and testing of cellular therapeutic products
  • 18/30375106 DC BS EN 14128. Durability of wood and wood-based products. Efficacy criteria for curative wood preservatives as determined by biological tests
  • BS EN ISO 10993-12:2007 Biological evaluation of medical devices - Sample preparation and reference materials
  • BS EN ISO 10993-12:2012 Biological evaluation of medical devices. Sample preparation and reference materials
  • 19/30354962 DC BS ISO 21973. Biotechnology. General requirements for transportation of cells for therapeutic use
  • BS ISO 23033:2021 Biotechnology. Analytical methods. General requirements and considerations for the testing and characterization of cellular therapeutic products
  • BS 5213:1975 Specification for medical specimen containers for microbiology
  • BS DD ISO/TS 11080:2009 Dentistry - Essential characteristics of test methods for the evaluation of treatment methods intended to improve or maintain the microbiological quality of dental unit procedural water
  • BS EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Biological indicators for dry heat sterilization processes
  • BS EN ISO 11138-1:2006 Sterilization of health care products - Biological indicators - General requirements
  • BS EN ISO 10993-12:2021 Tracked Changes. Biological evaluation of medical devices. Sample preparation and reference materials
  • BS EN ISO 11138-2:2006 Sterilization of health care products - Biological indicators - Biological indicators for ethylene oxide sterilization processes
  • BS EN ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Biological indicators for moist heat sterilization processes
  • BS EN ISO 11138-3:2009 Sterilization of health care products - Biological indicators - Biological indicators for moist heat sterilization processes
  • BS EN ISO 11138-3:2017 Sterilization of health care products. Biological indicators. Biological indicators for moist heat sterilization processes
  • BS EN ISO 23500-4:2019 Tracked Changes. Preparation and quality management of fluids for haemodialysis and related therapies. Concentrates for haemodialysis and related therapies
  • BS EN 12442-1:2000 Animal tissues and their derivatives utilized in the manufacture of medical devices - Analysis and management of risk
  • PD CEN/TS 17708:2022 Plant biostimulants. Preparation of sample for microbial analysis
  • PD CEN/TS 17702-2:2022 Plant biostimulants. Sampling and sample preparation. Sample preparation
  • BS EN ISO 11138-2:2009 Sterilization of health care products - Biological indicators - Biological indicators for ethylene oxide sterilization processes
  • BS EN ISO 11138-2:2017 Sterilization of health care products. Biological indicators. Biological indicators for ethylene oxide sterilization processes
  • BS EN ISO 11138-5:2006 Sterilization of health care products - Biological indicators - Biological indicators for low-temperature steam and formaldehyde sterilization processes
  • BS EN ISO 11138-8:2021 Sterilization of health care products. Biological indicators. Biological indicators for low-temperature steam and formaldehyde sterilization processes
  • PD ISO/TR 24290:2023 Health informatics. Datasets and data structure for clinical and biological evaluation metrics in radiotherapy
  • BS EN ISO 14780:2017 Solid biofuels. Sample preparation
  • BS EN 14780:2011 Solid biofuels. Sample preparation
  • BS EN ISO 14780:2017+A1:2019 Solid biofuels. Sample preparation
  • BS EN ISO 10993-17:2009 Biological evaluation of medical devices. Establishment of allowable limits for leachable substances
  • BS EN 1174-1:1996 Sterilization of medical devices - Estimation of the population of micro-organisms on product - Requirements
  • 19/30376763 DC BS EN ISO 10993-12. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials
  • BS EN 12689:1998 Biotechnology - Guidance on assessment of the purity, biological activity and stability of micro-organism based products
  • BS EN ISO 22442-2:2015 Medical devices utilizing animal tissues and their derivatives. Controls on sourcing, collection and handling
  • BS EN ISO 22442-2:2008 Medical devices utilizing animal tissues and their derivatives - Controls on sourcing, collection and handling
  • BS EN ISO 22442-2:2020 Medical devices utilizing animal tissues and their derivatives. Controls on sourcing, collection and handling
  • BS EN 1174-2:1997 Sterilization of medical devices - Estimation of the population of micro-organisms on product - Guidance
  • BS DD CEN/TS 14780:2005 Solid biofuels — Methods for sample preparation
  • BS DD CEN/TS 14780:2006 Solid biofuels. Methods for sample preparation
  • BS EN ISO 14160:2011 Sterilization of health care products. Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives. Requirements for characterization, development, validation and routine control of a sterilization proc
  • BS ISO 19984-2:2017 Rubber and rubber products. Determination of biobased content. Biobased carbon content
  • PD CEN/TS 17702-1:2022 Plant biostimulants. Sampling and sample preparation. Sampling
  • BS EN ISO 17511:2003 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials
  • PD ISO/TS 22456:2021 Sterilization of healthcare products. Microbiological methods. Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products
  • BS EN ISO 10993-9:1999 Biological evaluation of medical devices - Framework for identification and quantification of potential degradation products
  • BS EN ISO 6887-5:2020 Microbiology of the food chain. Preparation of test samples, initial suspension and decimal dilutions for microbiological examination - Specific rules for the preparation of milk and milk products
  • BS ISO 19984-3:2017 Rubber and rubber products. Determination of biobased content - Biobased mass content
  • BS EN 1174-3:1997 Sterilization of medical devices - Estimation of the population of micro-organisms on product - Guide to the methods for validation of microbiological techniques
  • 23/30463108 DC BS EN 17702-2. Plant biostimulants. Sampling and sample preparation - Part 2. Sample preparation
  • BS EN 17425:2021 Foodstuffs. Determination of ergot alkaloids in cereals and cereal products by dSPE clean-up and HPLC-MS/MS
  • BS EN 14065:2002 Textiles - Laundry processed textiles - Biocontamination control system

American Society for Testing and Materials (ASTM), Treatment + Biological Products + Products

  • ASTM F1600-95a(2001) Standard Terminology Relating to Bioremediation
  • ASTM F1600-95a Standard Terminology Relating to Bioremediation
  • ASTM F1600-95a(2007) Standard Terminology Relating to Bioremediation
  • ASTM F1834-98 Standard Guide for Consideration of Anaerobic Bioremediation as a Chemical Pollutant Mitigation Method on Land
  • ASTM F1834-98(2004) Standard Guide for Consideration of Anaerobic Bioremediation as a Chemical Pollutant Mitigation Method on Land
  • ASTM E2363-23 Standard Terminology Relating to Manufacturing of Pharmaceutical and Biopharmaceutical Products in the Pharmaceutical and Biopharmaceutical Industry

HU-MSZT, Treatment + Biological Products + Products

Association Francaise de Normalisation, Treatment + Biological Products + Products

  • NF EN ISO 16954:2015 Médecine bucco-dentaire - Méthodes d'essai pour le traitement du biofilm dans les conduites d'eau de l'unit dentaire
  • NF S99-512:2008 Biological evaluation of medical devices - Part 12 : sample preparation and reference materials.
  • NF X40-110:2004 Durability of wood and wood-based products - Performance criteria for curative wood preservatives as determined by biological tests.
  • NF EN ISO 10993-12:2021 Evaluation biologique des dispositifs médicaux - Partie 12 : préparation des échantillons et matériaux de référence
  • NF S99-501-12:2012 Biological evaluation of medical devices - Part 12 : sample preparation and reference materials.
  • NF S99-501-12*NF EN ISO 10993-12:2021 Biological evaluation of medical devices - Part 12 : sample preparation and reference materials
  • FD X40-111*FD CEN/TR 15003:2013 Durability of wood and wood-based products - Criteria for hot air processes for curative uses against wood destroying organisms
  • NF S93-305-4*NF EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4 : concentrates for haemodialysis and related therapies
  • NF S98-004-3:2006 Sterilization of health care products - Biological indicators - Part 3 : biological indicators for moist heat sterilization processes.
  • XP U45-026*XP CEN/TS 17708:2022 Plant biostimulants - Preparation of sample for microbial analysis
  • FD CEN/TR 15003:2013 Durabilité du bois et des matériaux dérivés du bois - Critères s'appliquant aux procédés à air chaud à usages curatifs contre les organismes lignivores
  • NF V08-501:1984 Food microbiology. Margarine. Preparation of a sample for microbiological analysis.
  • NF S98-004-2:2006 Sterilization of health care products - Biological indicators - Part 2 : biological indicators for ethylene oxide sterilization processes.
  • NF S98-118-1:2006 Sterilization of medical devices - Microbiological methods - Part 1 : determination of a population of microorganisms on products.
  • NF X34-122*NF EN ISO 14780:2017 Solid biofuels - Sample preparation
  • NF EN ISO 14780:2017 Biocombustibles solides - Préparation des échantillons
  • NF EN ISO 10993-17:2009 Évaluation biologique des dispositifs médicaux - Partie 17 : établissement des limites admissibles des substances relargables
  • NF S98-004-4:2006 Sterilization of health care products - Biological indicators - Part 4 : biological indicators for dry heat sterilization processes.
  • XP CEN/TS 17702-2:2022 Biostimulants des végétaux - Echantillonnage et préparation des échantillons - Partie 2 : préparation des échantillons
  • NF X42-312*NF EN 12689:1998 Biotechnology. Guidance on assessment of the purity, biological activity and stability of microorganism based products.
  • NF T51-022:1997 Plastics. Evaluation of the action of microorganisms.
  • NF S98-004-1:2006 Sterilization of health care products - Biological indicators - Part 1 : general requirements.
  • NF S98-112*NF EN ISO 14160:2021 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • NF S98-112:2011 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • NF EN 14128:2020 Durabilité du bois et des matériaux dérivés du bois - Efficacité des produits curatifs de préservation du bois établis par des essais biologiques
  • NF EN ISO 13969:2004 Lait et produits laitiers - Lignes directrices pour une description normalisée des méthodes microbiologiques de dépistage d'inhibiteurs microbiens
  • NF S98-100:2009 Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results.
  • NF EN ISO 6887-6:2013 Microbiologie des aliments - Préparation des échantillons, de la suspension mère et des dilutions décimales en vue de l'examen microbiologique - Partie 6 : règles spécifiques pour la préparation des échantillons prélevés au stade de producti...
  • NF V08-010-2:2004 Microbiology of food and animal feeding stuffs - Preparation of test samples, initial suspension and decimal dilutions for microbiological examination - Part 2 : specific rules for the preparation of meat and meat products.

European Committee for Standardization (CEN), Treatment + Biological Products + Products

  • PD CEN/TR 15003:2012 Durability of wood and wood-based products - Criteria for hot air processes for curative uses against wood destroying organisms
  • EN ISO 10993-12:2021 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
  • EN ISO 10993-12:1996 Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials ISO 10993-12 : 1996
  • EN 14128:2003 Durability of wood and wood-based products - Performance criteria for curative wood preservatives as determined by biological tests
  • EN 14128:2020 Durability of wood and wood-based products - Efficacy criteria for curative wood preservatives as determined by biological tests
  • EN 14780:2011 Solid biofuels - Sample preparation
  • EN ISO 16954:2015 Dentistry - Test methods for dental unit waterline biofilm treatment (ISO 16954:2015)
  • EN 14065:2016 Textiles - Laundry processed textiles - Biocontamination control system
  • EN ISO 17516:2014 Cosmetics - Microbiology - Microbiological limits
  • FprCEN/TS 17708-2021 Plant biostimulants - Preparation of sample for microbial analysis
  • EN ISO 11737-1:2018 Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products
  • CEN EN ISO 10993-12:2004 Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials ISO 10993-12:2002
  • EN 12689:1998 Biotechnology - Guidance on assessment of the purity, biological activity and stability of microorganism based products
  • EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • EN ISO 10993-8:2000 Biological Evaluation of Medical Devices - Part 8: Selection and Qualification of Reference Materials for Biological Tests ISO 10993-8:2000
  • prEN 17702-2 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation
  • CEN/TS 17702-2:2022 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation
  • FprCEN/TS 17702-2-2021 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation
  • EN ISO 1927-5:2012 Monolithic (unshaped) refractory products - Part 5: Preparation and treatment of test pieces (ISO 1927-5:2012)
  • EN 1174-3:1996 Sterilization of Medical Devices - Estimation of the Population of Micro-Organisms on Product - Part 3: Guide to the Methods for Validation of Microbiological Techniques
  • EN ISO 11138-1:2006 Sterilization of health care products - Biological indicators - Part 1: General requirements
  • EN 1174-1:1996 Sterilization of Medical Devices - Estimation of the Population of Micro- Organisms on Product - Part 1: Requirements
  • EN 1174-2:1996 Sterilization of Medical Devices - Estimation of the Population of Micro-Organisms on Product - Part 2: Guidance
  • EN 12442-2:2000 Animal Tissues and Their Derivatives Utilized in the Manufacture of Medical Devices - Part 2: Controls on Sourcing, Collection and Handling
  • EN ISO 11138-5:2006 Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes
  • EN ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • EN ISO 11737-1:2018/A1:2021 Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products - Amendment 1 (ISO 11737-1:2018/Amd 1:2021)
  • EN ISO 22442-2:2020 Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)

Tianjin Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB12/T 804-2018 Microbiological Standards for Water in Dental Comprehensive Treatment Units

US-CFR-file, Treatment + Biological Products + Products

  • CFR 21-1301.74-2014 Food and drugs. Part1301:Registration of manufacturers, distributors, and dispensers of controlled substances. Section1301.74:Other security controls for nonpractitioners; narcotic treatment programs and compounders for narcotic treatment programs.
  • CFR 21-1301.72-2014 Food and drugs. Part1301:Registration of manufacturers, distributors, and dispensers of controlled substances. Section1301.72:Physical security controls for nonpractitioners; narcotic treatment programs and compounders for narcotic treatment programs; sto
  • CFR 21-890.1-2013 Food and Drugs. Part890:Physical medicine devices. Section890.1:Scope.
  • CFR 21-890.3930-2013 Food and Drugs. Part890:Physical medicine devices. Section890.3930:Wheelchair elevator.
  • CFR 21-890.5150-2013 Food and Drugs. Part890:Physical medicine devices. Section890.5150:Powered patient transport.
  • CFR 21-316.23-2013 Food and drugs. Part316:Orphan drugs. Section316.23:Timing of requests for orphandrug designation; designation of already approved drugs.

German Institute for Standardization, Treatment + Biological Products + Products

  • DIN CEN/TR 15003:2012-11*DIN SPEC 68001:2012-11 Durability of wood and wood-based products - Criteria for hot air processes for curative uses against wood destroying organisms; German version CEN/TR 15003:2012
  • DIN EN 14128:2020 Durability of wood and wood-based products - Efficacy criteria for curative wood preservatives as determined by biological tests
  • DIN EN 14128:2020-06 Durability of wood and wood-based products - Efficacy criteria for curative wood preservatives as determined by biological tests; German version EN 14128:2020
  • DIN EN 14128:2004 Durability of wood and wood-based products - Performances criteria for curative wood preservatives as determined by biological tests; German version EN 14128:2003
  • DIN EN ISO 10993-12:2008 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007); German version EN ISO 10993-12:2007
  • DIN EN ISO 10993-12:2021-08 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021); German version EN ISO 10993-12:2021
  • DIN EN ISO 11137-2:2015-11 Dentistry - Test methods for dental unit waterline biofilm treatment (ISO 16954:2015); German version EN ISO 16954:2015
  • DIN EN ISO 16954:2015-11 Dentistry - Test methods for dental unit waterline biofilm treatment (ISO 16954:2015); German version EN ISO 16954:2015
  • DIN EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2006); English version of DIN EN ISO 11138-4:2006-09
  • DIN EN 17708:2023-05 Plant biostimulants - Preparation of sample for microbial analysis; German and English version prEN 17708:2023 / Note: Date of issue 2023-03-31*Intended as replacement for DIN CEN/TS 17708 (2022-07).
  • DIN CEN/TS 17708:2022-07 Plant biostimulants - Preparation of sample for microbial analysis; German version CEN/TS 17708:2022
  • DIN EN ISO 11138-1:2006 Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2006); English version of DIN EN ISO 11138-1:2006-09
  • DIN EN ISO 14780:2020-02 Solid biofuels - Sample preparation (ISO 14780:2017 + Amd 1:2019); German version EN ISO 14780:2017 + A1:2019
  • DIN EN ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006); German version EN ISO 11138-3:2006
  • DIN EN ISO 10993-12:2019 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO/DIS 10993-12:2019); German and English version prEN ISO 10993-12:2019
  • DIN EN ISO 11138-5:2006 Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2006); German version EN ISO 11138-5:2006
  • DIN EN 17702-2:2023 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation; German and English version prEN 17702-2:2023
  • DIN EN 17702-2:2023-04 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation; German and English version prEN 17702-2:2023 / Note: Date of issue 2023-03-17*Intended as replacement for DIN CEN/TS 17702-2 (2022-06).
  • DIN CEN/TS 17702-2:2022-06 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation; German version CEN/TS 17702-2:2022
  • DIN EN ISO 11138-2:2006 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2006); German version EN ISO 11138-2:2006
  • DIN EN 14735 Berichtigung 1:2006 Characterization of waste - Preparation of waste samples for ecotoxicity tests; German version EN 14735:2005, Corrigenda to DIN EN 14735:2005-11; German version EN 14735:2005/AC:2006
  • DIN EN ISO 14160:2018 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • DIN EN ISO 14160:2011 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • DIN EN ISO 16954:2015 Dentistry - Test methods for dental unit waterline biofilm treatment (ISO 16954:2015); German version EN ISO 16954:2015
  • DIN EN ISO 10993-12:2012 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012); German version EN ISO 10993-12:2012
  • DIN EN ISO 6887-4:2012 Microbiology of food and animal feeding stuffs - Preparation of test samples, initial suspension and decimal dilutions for microbiological examination - Part 4: Specific rules for the preparation of products other than milk and milk products, meat and mea
  • DIN EN 14735:2022-08 Characterization of waste - Preparation of waste samples for ecotoxicity tests; German version EN 14735:2021
  • DIN EN 15136:2006-06 Materials and articles in contact with foodstuffs - Certain epoxy derivatives subject to limitation - Determination of BADGE, BFDGE and their hydroxy and chlorinated derivatives in food simulants; German version EN 15136:2006

RU-GOST R, Treatment + Biological Products + Products

  • GOST R 57106-2016 Products diet therapeutic and preventive nutrition diet. Complexes vitamin-mineral in clinical nutrition. Specification
  • GOST 33275-2015 Biological medicine remedies for veterinary use. Vaccines fowl pox. Specifications
  • GOST R 55481-2013 Meat and meat products. Qualitative method for detection of antibiotics residues and other antimicrobial chemotherapeutic agents
  • GOST R ISO 10993-12-1999 Medical devices. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials
  • GOST ISO 10993-12-2011 Medical devices. Biological evaluation of medical devices. Part 12. Sample preparation and control materials
  • GOST ISO 10993-12-2015 Medical devices. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials
  • GOST 33933-2016 Products diet therapeutic and preventive nutrition diet. Protein complex dry blends. General specifications
  • GOST R ISO 11138-3-2000 Sterilization of health care products. Biological indicators. Part 3. Biological indicators for moist heat sterilization
  • GOST R 57298-2016 Radiopharmaceutical medicinal products. General requirements for organization of production of radiopharmaceuticals in medical organizations
  • GOST ISO 11138-3-2012 Sterilization of health care products. Biological indicators. Part 3. Biological indicators for moist heat sterilization
  • GOST ISO 11737-1-2012 Sterilization of medical devices. Microbiological methods. Part 1. Estimation of population of microorganisms on products
  • GOST R ISO 11737-1-2000 Sterilization of medical devices. Microbiological methods. Part 1. Estimation of population of microorganisms on products
  • GOST R ISO 11140-1-2000 Sterilization of health care products. Chemical indicators. Part 1. General requirements
  • GOST 30324.5-1995 Medical electrical equipment. Part 2. Particular requirements for safety of ultrasonic therapy equipment
  • GOST R ISO 13683-2000 Sterilization of health care products. Requirements for validation and routine control of moist heat sterilization in health care facilities
  • GOST ISO 11138-1-2012 Sterilization of health care products. Biological indicators. Part 1. Technical requirements
  • GOST R ISO 11138-1-2000 Sterilization of health care products. Biological indicators. Part 1. General requirements
  • GOST ISO 11138-2-2012 Sterilization of health care products. Biological indicators. Part 2. Biological indicators for ethylene oxide sterilization
  • GOST R ISO 11138-2-2000 Sterilization of health care products. Biological indicators. Part 2. Biological indicators for ethylene oxide sterilization
  • GOST 30364.1-1997 Egg products. Physical and chemical testing methods
  • GOST 32901-2014 Milk and milk products. Methods of microbiological analysis
  • GOST 32923-2014 Fermented milk products enriched with probiotic microorganisms. Specifications
  • GOST R 52711-2007 Manufacturing of juice products. Microbiological control methods using special microbiological nutrient media
  • GOST R 52711-2006 Manufacturing of juice products. Microbiological controlmethods using specialmicrobiological nutrient media
  • GOST R 52770-2007 Medical products. Safety requirements. Methods of sanitation-chemical and toxicological tests
  • GOST R ISO 18472-2009 Sterilization of health care products. Biological and chemical indicators. Test equipment
  • GOST 33255-2015 Solid biofuels. Methods for sample preparation
  • GOST R 54212-2010 Solid biofuels. Methods for sample preparation
  • GOST 4.13-1989 Qnalitu ratind sustem. Smallwaresfor domestic use. Qualitu charateristics namenelature
  • GOST 31502-2012 Milk and milk products. Microbiological methods of the determination of antibiotics

IT-UNI, Treatment + Biological Products + Products

  • UNI ISO 21973:2021 Biotechnology - General requirements for transportation of cells for therapeutic use
  • UNI EN ISO 10993-12:2021 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • UNI EN ISO 14160:2021 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr

KR-KS, Treatment + Biological Products + Products

  • KS J ISO 21973-2023 Biotechnology — General requirements for transportation of cells for therapeutic use
  • KS J ISO TS 20399-2-2019 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 2: Best practice guidance for ancillary material suppliers
  • KS J ISO TS 20399-3-2019 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 3: Best practice guidance for ancillary material users
  • KS P ISO 11737-1-2018 Sterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on products
  • KS M ISO 14780-2021 Solid biofuels — Sample preparation
  • KS P ISO 10993-13-2018 Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices

VN-TCVN, Treatment + Biological Products + Products

  • TCVN 7391-12-2007 Biological evaluation of medical devices.Part 12: Sample preparation and reference materials

Danish Standards Foundation, Treatment + Biological Products + Products

  • DS/ISO/TS 23565:2021 Biotechnology – Bioprocessing – General requirements and considerations for equipment systems used in the manufacturing of cells for therapeutic use
  • DS/ISO/TS 22456:2021 Sterilization of healthcare products – Microbiological methods – Guidance on conducting bioburden determinations and tests of sterility for biologics and tissue-based products
  • DS/ISO 10993-12:2021 Biological evaluation of medical devices – Part 12: Sample preparation and reference materials
  • DS/EN ISO 10993-12:2012 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • DS/ISO 23033:2021 Biotechnology – Analytical methods – General requirements and considerations for the testing and characterization of cellular therapeutic products
  • DS/CEN/TR 15003:2013 Durability of wood and wood-based products - Criteria for hot air processes for curative uses against wood destroying organisms
  • DS/EN ISO 10993-12:2021 Biological evaluation of medical devices – Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
  • DS/EN ISO 11737-1/AC:2009 Sterilization of medical devices – Microbiological methods – Part 1: Determination of a population of microorganisms on products
  • DS/EN ISO 11737-1:2006 Sterilization of medical devices – Microbiological methods – Part 1: Determination of a population of microorganisms on products
  • DS/EN 14780:2011 Solid biofuels - Sample preparation
  • DS/EN ISO 14160:2011 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • DS/EN 15136:2006 Materials and articles in contact with foodstuffs - Certain epoxy derivatives subject to limitation - Determination of BADGE, BFDGE and their hydroxy and chlorinated derivatives in food simulants

CEN - European Committee for Standardization, Treatment + Biological Products + Products

  • PREN 14128-2018 Durability of wood and wood-based products - Efficacy criteria for curative wood preservatives as determined by biological tests
  • EN ISO 10993-12:2009 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • EN ISO 10993-12:2007 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • EN ISO 10993-12:2012 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • EN ISO 10993-12:2004 Biological Evaluation of Medical Devices - Part 12: Sample Preparation and Reference Materials
  • PD CEN/TS 14780:2005 Solid biofuels - Methods for sample preparation
  • EN ISO 22442-2:2007 Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing@ collection and handling

ES-UNE, Treatment + Biological Products + Products

  • UNE-EN 14128:2020 Durability of wood and wood-based products - Efficacy criteria for curative wood preservatives as determined by biological tests
  • UNE-EN ISO 16954:2015 Dentistry - Test methods for dental unit waterline biofilm treatment (ISO 16954:2015)
  • UNE-EN ISO 10993-12:2022 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
  • UNE-CEN/TS 17708:2022 Plant biostimulants - Preparation of sample for microbial analysis (Endorsed by Asociación Española de Normalización in May of 2022.)
  • UNE-EN ISO 14780:2018 Solid biofuels - Sample preparation (ISO 14780:2017)
  • UNE-CEN/TS 17702-2:2022 Plant biostimulants - Sampling and sample preparation - Part 2: Sample preparation (Endorsed by Asociación Española de Normalización in May of 2022.)
  • UNE-EN 14735:2021 Characterization of waste - Preparation of waste samples for ecotoxicity tests (Endorsed by Asociación Española de Normalización in January of 2022.)
  • UNE-EN 15136:2006 Materials and articles in contact with foodstuffs - Certain epoxy derivatives subject to limitation - Determination of BADGE, BFDGE and their hydroxy and chlorinated derivatives in food simulants (Endorsed by AENOR in May of 2006.)

Group Standards of the People's Republic of China, Treatment + Biological Products + Products

  • T/SHPPA 019-2023 Guidance for the manufacturing quality management of plasmids used in the production of Immune cell therapy products
  • T/CMBA 021-2023 Specification of quality management for ancillary materials present during the production of cellular therapeutic products
  • T/CAPC 006-2022 Standardized method for pharmaceutical care of pharmacies retailing assisted reproductive technology drug
  • T/SHPPA 021-2023 Import and export management guidance for CAR-T cell therapy products and their materials
  • T/CAMDI 034-2020 Biological evaluation of medical devices Medical catheter with hydrophilic polymer coating：Sample preparation
  • T/SHPPA 002-2020 General Technical Guideline for the Quality Evaluation and Standard Development of Narrow Therapeutic Index Drugs
  • T/SHPPA 007-2020 General Technical Guideline for the Quality Evaluation and Standard Development of Narrow Therapeutic Index Drugs
  • T/GDCDC 011-2019 Microbiological Control Standard for Cosmetic Product manufactures
  • T/CAPDA 027-2022 Code of practice for control of forage grass root rot disease using plant microecological Bacillus preparation
  • T/JGE 0016-2022 Jiangxi Green Ecological Brewed Cereal Products
  • T/JGE 0016-2023 Jiangxi Green Ecology—Prepared grain products
  • T/CAPDA 026-2022 Code of practice for control of brown patch disease in turfgrass using plant microecological Bacillus preparation

Japanese Industrial Standards Committee (JISC), Treatment + Biological Products + Products

  • JIS T 5111:2018 Dentistry -- Test methods for dental unit waterline biofilm treatment
  • JIS T 11737-1:2013 Sterilization of medical devices.Microbiological methods.Part 1: Determination of a population of microorganisms on products
  • JIS T 9010:1999 Test methods relevant to biological safety of rubber products

Canadian General Standards Board （CGSB), Treatment + Biological Products + Products

  • CGSB 43.125-2003-CAN/CGSB-2003 Conception Et Fabrication Des Emballages Destines Au Transport Des Materes Infectieuses, Des Echantillons De Diagnostic, Des Produits Biologieques Et Des Dechets Biomedicaux
  • CAN/CGSB-43.125-2016 Packaging of Category A and Category B infectious substances (Class 6.2) and clinical, (bio) medical or regulated medical waste

TH-TISI, Treatment + Biological Products + Products

  • TIS 2395.12-2008 Biological evaluation of medical devices.part 12: sample preparation and reference materials
  • TIS 2395.13-2008 Biological evaluation of medical devices.part 13: identification and quantification of degradation products from polymeric medical devices

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, Treatment + Biological Products + Products

  • GB/T 16886.12-2005 Biological evaluation of medical devices-Part 12:Sample preparation and reference materials
  • GB/T 16886.12-2000 Biological evaluation of medical devices--Part 12: Sample preparation and reference materials
  • GB 18281.3-2000 Sterilization of health care products--Biological indicators--Part 3: Biological indicators for moist heat sterilization
  • GB 18281.4-2015 Biological indicators for sterilization of healthcare products - Part 4: Biological indicators for dry heat sterilization
  • GB 18281.3-2015 Biological indicators for sterilization of healthcare products - Part 3: Biological indicators for moist heat sterilization
  • GB 18281.1-2000 Sterilization of health care products--Biological indicators--Part 1: General
  • GB 18281.1-2015 Sterilization of health care products.Biological indicators.Part 1:General requirements
  • GB/T 19973.1-2023 Microbiological methods for sterilization of healthcare products - Part 1: Determination of the total number of microorganisms on products
  • GB 18281.2-2000 Sterilization of health care products--Biological indicators--Part 2: Biological indicators for ethylene oxide sterilization
  • GB 18281.2-2015 Biological indicators for sterilization of healthcare products - Part 2: Biological indicators for ethylene oxide sterilization
  • GB 16383-2014 Quality control for radiation sterilization of medical and hygienical products
  • GB/T 24628-2009 Sterilization of health care products.Biological and chemical indicators.Test equipment
  • GB/T 21415-2008 In vitro diagnostic medical devices.Measurement of quantities in biological samples.Metrological traceability of values assigned to calibrators and control materials
  • GB 18281.5-2015 Biological indicators for sterilization of healthcare products - Part 5: Biological indicators for formaldehyde sterilization by low temperature steam
  • GB/T 4789.19-2003 Microbiological examination of food hygiene Examination of egg and egg products
  • GB 4789.18-1994 Microbiological examination of food hygiene.Examination of milk and milk products
  • GB/T 4789.17-2003 Microbiological examination of food hygiene Examination of meat and meat products
  • GB/T 4789.18-2003 Microbiological examination of food hygiene Examination of milk and milk products
  • GB 16383-1996 Quality control standards for radiation sterilization of medical and hygienical products
  • GB 10136-2005 Hygienic standard for salt & liquor-saturated aquatic products of animal origin
  • GB/T 19973.1-2015 Sterilization of medical devices.Microbiological methods.Part 1:Determination of a population of microorganisms on products
  • GB/T 4789.23-2003 Microbiological examination of food hygiene Examination of cold dish and bean products
  • GB 10144-2005 Hygienic standard for dried aquatic products of animal origin
  • GB/T 19972-2005 Sterilization of health care products.Biological indicators.Guidance for the selection, use and interpretation of results
  • GB/T 19703-2005 In vitro diagnostic medical devices-Measurement of quantities in samples of biological origin-Description of reference materials
  • GB/T 28730-2012 Method for preparation of solid biofuels sample

Professional Standard - Medicine, Treatment + Biological Products + Products

  • YY/T 1411-2016 Dentistry.Essential characteristics of test methods for the evaluation of treatment methods intended to improve or maintain the microbiological quality of dental unit procedural water
  • YY/T 1411-2016/ISO/TS 11080:2009 Dentistry test method for evaluating measures to improve or maintain the microbiological quality of water used in dental units
  • YY 0793.3-2023 Preparation and quality control of fluids for hemodialysis and related treatments - Part 3: Concentrates for hemodialysis and related treatments
  • YY/T 0638-2008 In vitro diagnostic medical devices.Measurement of quantities in biological samples.Metrological traceability of assigned values for catalytic concentration of enzymes in calibrators and control materials
  • YY/Y 1576-2017 Implantation Test of Absorbable Biomaterials for Tissue Engineering Medical Devices

Korean Agency for Technology and Standards (KATS), Treatment + Biological Products + Products

  • KS P ISO 16954:2017 Dentistry ─ Test methods for dental unit waterline biofilm treatment
  • KS P ISO 10993-12:2007 Biological evaluation of medical devices-Part 12:Sample preparation and reference materials
  • KS P ISO 10993-12:2014 Biological evaluation of medical devices — Part 12: Sample preparation and reference materials
  • KS P ISO 10993-12-2014(2019) Biological evaluation of medical devices —Part 12: Sample preparation and reference materials
  • KS J ISO TS 20399-2:2019 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 2: Best practice guidance for ancillary material suppliers
  • KS J ISO TS 20399-3:2019 Biotechnology — Ancillary materials present during the production of cellular therapeutic products — Part 3: Best practice guidance for ancillary material users
  • KS P ISO 11737-1:2012 Sterilization of medical devices－Microbiological methods－Part 1：Determination of population of microorganisms on products
  • KS P ISO 11737-1:2018 Sterilization of medical devices — Microbiological methods — Part 1: Determination of a population of microorganisms on products
  • KS P ISO 11138-2:2012 Sterilization of health care products－Biological indicators－Part 2：Biological indicators for ethylene oxide sterilization processes
  • KS M ISO 14780:2021 Solid biofuels — Sample preparation
  • KS P ISO 10993-13:2018 Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
  • KS P ISO 14161:2012 Sterilization of health care products－Biological indicators－Guidance for the selection, use and interpretation of results
  • KS P ISO 22442-2:2010 Medical devices utilizing animal tissues and their derivatives－Part 2：Controls on sourcing, collection and handling

国家药监局, Treatment + Biological Products + Products

  • YY/T 1411-2023 Test method for biofilm treatment in waterways of dental treatment machines in dentistry
  • YY/T 1737-2020 Analytical methods for bioburden control levels of medical devices

North Atlantic Treaty Organization Standards Agency, Treatment + Biological Products + Products

  • STANAG 2242-2005 POLICY FOR THE CHEMOPROPHYLAXIS AND IMMUNOTHERAPY OF NATO PERSONNEL AGAINST BIOLOGICAL WARFARE AGENTS

Taiwan Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • CNS 14393.12-2005 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • CNS 14393-12-2005 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials

AENOR, Treatment + Biological Products + Products

  • UNE-CEN/TR 15003:2013 IN Durability of wood and wood-based products - Criteria for hot air processes for curative uses against wood destroying organisms
  • UNE 315500:2017 Inputs to be used in organic plant production. Products for pest and disease management.
  • UNE-EN ISO 10993-12:2013 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)
  • UNE-EN 14780:2012 Solid biofuels - Sample preparation
  • UNE-EN ISO 11737-1:2007 Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006)
  • UNE-EN ISO 14160:2012 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr

US-FCR, Treatment + Biological Products + Products

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, Treatment + Biological Products + Products

  • GB/T 16886.12-2017 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
  • GB/T 19972-2018 Sterilization of health care products—Biological indicators—Guidance for the selection, use and interpretation of results

Beijing Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB11/T 1330-2016 Application Technical Regulations for Biological Control Products
  • DB11/ 614-2009 Hygienic requirements for cereal flour products
  • DB11/T 1602-2018 Application technical regulations of biological control products
  • DB11/T 2094-2023 Technical regulations for artificial breeding and application of biological control products
  • DB11/T 1129-2014 Application technical regulations of biological control products
  • DB11/T 1432-2017 Technical regulations for the application of biological control products Gypsy moth nuclear polyhedrosis virus
  • DB11/T 900-2012 Cold chain technical specification for veterinary biological products

US-AAMI, Treatment + Biological Products + Products

  • ANSI/AAMI/ISO 10993-12:2007 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials
  • AAMI TIR37-2013 Sterilization of health care products - Radiation - Guidance on sterilization of biologics and tissue-based products

US-CLSI, Treatment + Biological Products + Products

  • CLSI I/LA34-P-2010 Design and Validation of Immunoassays for Assessment of Human allergenicity of New Biotherapeutic Drugs
  • CLSI I/LA34-A-2011 Design and Validation of Immunoassays for Assessment of Human Allergenicity of New Biotherapeutic Drugs; Approved Guideline

UNKNOWN, Treatment + Biological Products + Products

  • GB/T 18281.3-2015 Biological Indicators for Sterilization of Healthcare Products Part 3: Biological Indicators for Moist Heat Sterilization
  • GB/T 18281.4-2015 Biological Indicators for Sterilization of Healthcare Products Part 4: Biological Indicators for Dry Heat Sterilization
  • GB/T 18281.2-2015 Biological indicators for sterilization of healthcare products - Part 2: Biological indicators for ethylene oxide sterilization
  • GB/T 18281.5-2015 Biological Indicators for Sterilization of Healthcare Products Part 5: Biological Indicators for Formaldehyde Sterilization by Low Temperature Steam

American National Standards Institute （ANSI), Treatment + Biological Products + Products

  • ANSI/AAMI/ISO 11737-1:2006 Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products
  • ANSI/AAMI/ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • ANSI/AAMI/ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • ANSI/AAMI/ISO 11138-5:2006 Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes
  • ANSI/AAMI/ISO 11138-2:2006 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes
  • ANSI/AAMI/ISO 11138-1:2006 Sterilization of health care products - Biological indicators - Part 1: General requirements
  • ANSI/AAMI/ISO 22442-2:2007 Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling

Jiangsu Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB32/T 4529-2023 Technical operating procedures for vector control in medical institutions

AT-ON, Treatment + Biological Products + Products

  • ONR CEN/TS 17708-2021 Plant biostimulants - Preparation of sample for microbial analysis
  • OENORM EN ISO 10993-12:2021 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
  • OENORM EN ISO 14160:2021 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • ONORM DIN 10191-3-1992 Microbiological analysis of milk - Preparation of samples - Method for milk tat products

PL-PKN, Treatment + Biological Products + Products

Association of German Mechanical Engineers, Treatment + Biological Products + Products

  • VDI 3787 Blatt 10-2010 Environmental meteorology - Human biometeorological requirements in the framework of recreation, prevention, therapy, and rehabilitation

ET-QSAE, Treatment + Biological Products + Products

CH-SNV, Treatment + Biological Products + Products

  • SN EN ISO 10993-12:2021 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
  • SN EN ISO 14160:2021 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • SN EN ISO 6887-3/A1:2021 Microbiology of the food chain - Preparation of test samples, initial suspension and decimal dilutions for microbiological examination - Part 3: Specific rules for the preparation of fish and fishery products - Sample preparation for raw marine gastropods

Lithuanian Standards Office , Treatment + Biological Products + Products

  • LST EN ISO 10993-12:2021 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
  • LST EN 14780-2011 Solid biofuels - Sample preparation
  • LST EN ISO 11737-1:2006 Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006)
  • LST EN ISO 14160:2011 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • LST EN ISO 14160:2021 Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization pr
  • LST EN 15136-2006 Materials and articles in contact with foodstuffs - Certain epoxy derivatives subject to limitation - Determination of BADGE, BFDGE and their hydroxy and chlorinated derivatives in food simulants

未注明发布机构, Treatment + Biological Products + Products

CZ-CSN, Treatment + Biological Products + Products

  • CSN 56 0081-1983 Food products. reparation of samples for icrobiological examination
  • CSN 57 0165-1984 Canned foods. Preparation of samples for microbiological examination

中华人民共和国国家卫生和计划生育委员会, Treatment + Biological Products + Products

  • GBZ 178-2006 Specification for radiological protection and quality control in implanted treatment of low energy γ-ray seed sources

Standard Association of Australia （SAA）, Treatment + Biological Products + Products

  • AS 5013.20:2004 Food microbiology - Preparation of test samples for microbiological examination?Poultry and poultry products
  • AS 5013.11.4:2006 Food microbiology - Microbiology of food and animal feeding stuffs - Preparation of test samples, initial suspension and decimal dilutions for microbiological examination - Specific rules for the preparation of products other than milk and milk products,
  • AS 5013.11.5:2012
  • AS 5013.11.2:2006 Food microbiology - Microbiology of food and animal feeding stuffs - Preparation of test samples, initial suspension and decimal dilutions for microbiological examination - Specific rules for the preparation of meat and meat products
  • AS 5013.11.2:2017 Food microbiology, Part 11.2: Microbiology of the food chain — Preparation of test samples, initial suspension and decimal dilutions for microbiological examination — Specific rules for the preparation of meat and meat products
  • AS/NZS 2647:2000 Biological safety cabinets - Installation and use
  • AS 1766.3.12:1992 Food microbiology - Examination of specific products - Cultured dairy products
  • AS 5013.11.3:2012
  • AS 5013.11.4:2018 Food microbiology, Method 11.4: Microbiology of the food chain — Preparation of test samples, initial suspension and decimal dilutions for microbiological examination — Specific rules for the preparation of miscellaneous products (ISO 6887-4:2017, MOD)
  • AS 5013.20:2017 Food microbiology, Method 20: Preparation of test samples for microbiological examination — Poultry and poultry product surfaces
  • AS 5013.7:2004 Food microbiology - Examination of specific products - Eggs and egg products

IX-FAO, Treatment + Biological Products + Products

  • CAC/RCP 15-1976(En) Hygienic operating procedures for egg products (including microbiological requirements for sterilized egg products)

SE-SIS, Treatment + Biological Products + Products

RO-ASRO, Treatment + Biological Products + Products

  • SR 6349-13-1995 Milk and milk products. Microbiologycal conditions
  • STAS 6349/1-1980 MILK AND MILK PRODUC DUCTS Sampling and specimen preparation for microbiolo-gical analysis
  • STAS 10914-1989 PLASTIC MEDICAL ARTICLES AND DEVICES Analysis methods for biological compatibility evaluation
  • STAS 10668-1976 CEREALS, PULSES AND ERIVED PRODUCTS etermination of crude ash

农业农村部, Treatment + Biological Products + Products

GOSTR, Treatment + Biological Products + Products

  • GOST R 52770-2020 Medical devices. Evaluation system of biological effects. Part 1. General requirements for biological safety
  • GOST 7702.2.1-2017 Poultry slaughtering products, poultry meat products and environment production objects. The method of identification of mesophilic aerobic and facultative anaerobic microorganisms
  • GOST 34285-2017 Food products, food raw materials. Method for the detection of chemotherapeutic drugs by the hemiluminescence immunoenzymatic assay with the use of biochip technology
  • GOST 9225-1984 Milk and milk products. Methods of microbiological analysis

Canadian Standards Association (CSA), Treatment + Biological Products + Products

  • CSA Z11138-1-07-CAN/CSA-2007 St閞ilisation des produits de sant??Indicateurs biologiques ?Partie 1: Exigences g閚閞ales deuxi鑝e 閐ition

Xinjiang Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB65/T 2878-2008 Technical regulations for integrated control of major pests of green food table grapes

Shandong Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB37/T 3016-2017 Detailed rules for the investigation and management system of hidden dangers of production safety accidents in production and sales enterprises of civil explosives
  • DB37/T 3340-2018 Guidelines for the implementation of the inspection and management system for hidden dangers of production safety accidents in dairy products manufacturing enterprises

Sichuan Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB51/T 2965-2022 Species identification specification for endangered wild animals and their products
  • DB51/T 2966-2022 Species identification specification for endangered wild plants and their products

Professional Standard - Commodity Inspection, Treatment + Biological Products + Products

  • SN/T 3063.2-2015 Aviation Food Part 2: Specifications for Control of Microbial Contamination of Raw (Cut) Fruit and Vegetable Products
  • SN/T 1750-2006 Determination of antibiotics residues in animal derived food-MIA method

American Society of Heating, Refrigerating and Air-Conditioning Engineers (ASHRAE), Treatment + Biological Products + Products

PT-IPQ, Treatment + Biological Products + Products

  • NP 723-1989 Meat and meat products Sausage. Definition and characteristics
  • NP EN 1174-2-2000 Sterilization of medical devices Estimation of the population of micro-organisms on product Part 2:Guidance
  • NP EN 1174-3-2000 Sterilization of medical devices Estimation of the population of micro-organisms on product Part 3:Guide to the methods for validation of microbiological techniques

IL-SII, Treatment + Biological Products + Products

  • S.I.628-1966 MICROBIOLOGICAL TESTING OF MILK AND MILK PRODUCTS : SAMPLING

Hebei Provincial Standard of the People's Republic of China, Treatment + Biological Products + Products

  • DB13/T 1830-2013 Technical requirements for recycled products from construction waste

Professional Standard - Military and Civilian Products, Treatment + Biological Products + Products

  • WJ/T 9100-2022 Manufacturing and Marketing Enterprise of Civil Explosives Materials Production Risk Classification Management and Control System Construction Guide

卫生健康委员会, Treatment + Biological Products + Products

  • WS/T 691-2020 Vector biological control operating procedures for food production and processing enterprises

  Treatment + Biological Products + Products.

 



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