Commission Directive 2004/73/EC of 29 April 2004 adapting to technical progress for the twenty-ninth time Council Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances (Text with EEA relevance)
EU Directive 2004/73 · Adopted 29 April 2004 · Extends to United Kingdom
Commission Directive 2004/73/EC
of 29 April 2004
adapting to technical progress for the twenty-ninth time Council Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances
(Text with EEA relevance)
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 67/548/EEC of 27 June 1967 on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substancesf1, and in particular Article 28 thereof,
Whereas:
(1)
Annex I to Directive 67/548/EEC contains a list of dangerous substances, together with particulars of the classification and labelling of each substance. That list needs to be updated to include further notified new substances and further existing substances as well adapting the existing entries to technical progress such as setting environmental concentration limits for certain substances. Accordingly it is also necessary to delete entries for certain substances and to split some entries because the classification no longer applies to all the substances under those entries. The labelling of substances containing 1,3-butadiene should be changed in order to reflect that that substance will be classified as a mutagen by the present Directive.
(2)
Annex V to Directive 67/548/EEC lays down the methods for the determination of the physicochemical properties, toxicity and ecotoxicity of substances and preparations. It is appropriate to amend that Annex in order to obtain a reduction to a minimum of the number of animals used for experimental purposes, in accordance with Council Directive 86/609/EEC of 24 November 1986 on the approximation of laws, regulations and administrative provisions of the Member States regarding the protection of animals used for experimental and other scientific purposesf2. The methods for sub-chronic oral toxicity in Chapters B.1, B.4, B.5, B.31 and B.35 should be revised accordingly. Furthermore, Chapter B.42 should be added to Annex V in order to make available a refined method on sub-chronic oral toxicity. Finally, Chapter A.21 on physico-chemical properties, Chapter B.43 on sub-chronic oral toxicity and Chapters C.21 to C.24 on environmental toxicity should be added in order to allow for the determination of properties which are not yet sufficiently covered by the methods in Annex V.
(3)
The measures provided for in this Directive are in accordance with the opinion of the Committee on the Adaptation to Technical Progress of the Directives for the Elimination of Technical Barriers to Trade with Dangerous Substances and Preparations,
HAS ADOPTED THIS DIRECTIVE:
Annotations to the whole text
Footnotes
- f1
-
OJ 196,16.8.1967, p. 1. Directive as last amended by Commission Directive 2001/59/EC (OJ L 225, 6.8.2001, p. 1)
- f2
-
OJ L 358, 18.12.1986, p. 1. Directive as last amended by Directive 2003/65/EC of the European Parliament and of the Council (OJ L 230,16.9.2003, p. 32).
Contents
- 1Article 1
- 2Article 2
- 3Article 3
- 4Article 4
- Signature
- Annex 1AAnnex 1A
- Note K:
- Annex 2AAnnex 2A
- OXIDIZING PROPERTIES (LIQUIDS)
- METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS AND UNITS
- 1.3REFERENCE SUBSTANCE
- 1.4PRINCIPLE OF THE TEST METHOD
- 1.5QUALITY CRITERIA
- DESCRIPTION OF THE METHOD
- Preparation
- 1.6.1.1Combustible substance
- 1.6.1.2Apparatus
- 1.6.2Performance of the test
- 2DATA
- 2.1TREATMENT OF RESULTS
- REPORT
- 3.1TEST REPORT
- 3.2INTERPRETATION OF THE RESULTS
- REFERENCES
- (1)Division (1)
- Annex 2B
- ACUTE ORAL TOXICITY - FIXED DOSE PROCEDURE
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- 1.4.1Selection of animal species
- 1.4.2Housing and feeding conditions
- 1.4.3Preparation of animals
- 1.4.4Preparation of doses
- PROCEDURE
- 1.5.1Administration of doses
- 1.5.2Sighting study
- 1.5.3Main study
- 1.6OBSERVATIONS
- 1.6.1Body weight
- 1.6.2Pathology
- 2DATA
- REPORTING
- 3.1Test report
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- ANNEX 1: FLOW CHART FOR THE SIGHTING STUDY
- ANNEX 1: FLOW CHART FOR THE SIGHTING STUDY
- ANNEX 2: FLOW CHART FOR THE MAIN STUDY
- ANNEX 2: FLOW CHART FOR THE MAIN STUDY
- ANNEX 3
- CRITERIA FOR CLASSIFICATION OF TEST SUBSTANCES WITH EXPECTED LD50 VALUES EXCEEDING 2000 MG/KG WITHOUT THE NEED FOR TESTING.
- TESTING AT DOSES ABOVE 2000 MG/KG
- Sighting Study
- Main Study
- ANNEX 4:TEST METHOD B.1 bis - Guidance on classification according to the EU scheme to cover the transition period until full implementation of the Globally Harmonised Classification System (GHS) (taken from reference (8))
- ANNEX 4:TEST METHOD B. 1 bis - Guidance on classification according to the EU scheme to cover the transition period until full implementation of the Globally Harmonised Classification System (GHS) (taken from reference (8))
- Annex 2C
- ACUTE ORAL TOXICITY - ACUTE TOXIC CLASS METHOD
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3PRINCIPLE OF THE TEST
- DESCRIPTION OF THE METHOD
- 1.4.1Selection of animal species
- 1.4.2Housing and feeding conditions
- 1.4.3Preparation of animals
- 1.4.4Preparation of doses
- PROCEDURE
- 1.5.1Administration of doses
- 1.5.2Number of animals and dose levels
- 1.5.3Limit test
- 1.6OBSERVATIONS
- 1.6.1Body weight
- 1.6.2Pathology
- 2DATA
- REPORTING
- 3.1Test report
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- PROCEDURE TO BE FOLLOWED FOR EACH OF THE STARTING DOSES
- GENERAL REMARKS
- ANNEX 2
- CRITERIA FOR CLASSIFICATION OF TEST SUBSTANCES WITH EXPECTED LD50 VALUES EXCEEDING 2000 MG/KG WITHOUT THE NEED FOR TESTING
- TESTING AT DOSES ABOVE 2000 MG/KG
- Annex 2D
- ACUTE TOXICITY: DERMAL IRRITATION/CORROSION
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- Preparation for the in vivo test
- 1.4.1.1Selection of animal species
- 1.4.1.2Preparation of the animals
- 1.4.1.3Housing and feeding conditions
- Test procedure
- 1.4.2.1Application of the test substance
- 1.4.2.2Dose level
- 1.4.2.3Initial test (In vivo dermal irritation/corrosion test using one animal)
- 1.4.2.4Confirmatory test (In vivo dermal irritation test with additional animals)
- 1.4.2.5Observation period
- 1.4.2.6Clinical observations and grading of skin reactions
- DATA
- 2.1PRESENTATION OF RESULTS
- 2.2EVALUATION OF RESULTS
- REPORTING
- 3.1TEST REPORT
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (5a)Division (5a)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)EPA (1990). Atlas of Dermal Lesions, (20T-2004). United States Environmental Protection Agency, Office of Pesticides and Toxic Substances, Washington, DC, August 1990.
- TABLE I:GRADING OF SKIN REACTIONS
- A Sequential Testing Strategy for Dermal Irritation and Corrosion
- GENERAL CONSIDERATIONS
- DESCRIPTION OF THE EVALUATION AND TESTING STRATEGY
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- FIGURETESTING AND EVALUATION STRATEGY FOR DERMAL IRRITATION /CORROSION
- Annex 2E
- ACUTE TOXICITY: EYE IRRITATION/CORROSION
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- Preparation for the in vivo test
- 1.4.1.1Selection of species
- 1.4.1.2Preparation of animals
- 1.4.1.3Housing and feeding conditions
- Test procedure
- 1.4.2.1Application of the test substance
- 1.4.2.2Irrigation
- 1.4.2.3Dose level
- 1.4.2.4Initial test (In vivo eye irritation/corrosion test using one animal)
- 1.4.2.5Local anaesthetics
- 1.4.2.6Confirmatory test (In vivo eye irritation test with additional animals)
- 1.4.2.7Observation period
- DATA
- 2.2EVALUATION OF RESULTS
- REPORTING
- 3.1TEST REPORT
- 3.2INTERPRETATION OF THE RESULTS
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (6a)Division (6a)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- TABLE I: GRADING OF OCULAR LESIONS
- A Sequential Testing Strategy for Eye Irritation and Corrosion
- GENERAL CONSIDERATIONS
- DESCRIPTION OF THE STEPWISE TESTING STRATEGY
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- FIGURETESTING AND EVALUATION STRATEGY FOR EYE IRRITATION/CORROSION
- Annex 2F
- PRENATAL DEVELOPMENTAL TOXICITY STUDY
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3REFERENCE SUBSTANCE
- 1.4PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- 1.5.1Selection of animal species
- 1.5.2Housing and feeding conditions
- 1.5.3Preparation of the animals
- PROCEDURE
- 1.6.1Number and sex of animals
- 1.6.2Preparation of doses
- 1.6.3Dosage
- 1.6.4Limit test
- 1.6.5Administration of doses
- 1.6.6Observations of the dams
- 1.6.7Body weight and food consumption
- 1.6.8Post-mortem examination
- 1.6.9Examination of uterine contents
- 1.6.10Examination of foetuses
- DATA
- 2.1TREATMENT OF RESULTS
- 2.2EVALUATION OF RESULTS
- 2.3INTERPRETATION OF RESULTS
- REPORTING
- TEST REPORT
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- (13)Division (13)
- (14)Division (14)
- (15)Division (15)
- (16)Division (16)
- (17)Division (17)
- (18)Division (18)
- (19)Division (19)
- (20)Division (20)
- (21)Division (21)
- (22)Division (22)
- (23)Division (23)
- (24)Division (24)
- (25)Division (25)
- (26)Division (26)
- (27)Division (27)
- (28)Division (28)
- Annex 2G
- TWO-GENERATION REPRODUCTION TOXICITY STUDY
- 1METHOD
- 1.1INTRODUCTION
- 1.2PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- 1.3.1Selection of animal species
- 1.3.2Housing and feeding conditions
- 1.3.3Preparation of animals
- PROCEDURE
- 1.4.1Number and sex of animals
- 1.4.2Preparation of Doses
- 1.4.3Dosage
- 1.4.4Limit test
- 1.4.5Administration of doses
- 1.4.6Experimental schedules
- Mating procedure
- 1.4.7.1Parental (P) mating
- 1.4.7.2F1 mating
- 1.4.7.3Second mating
- 1.4.7.4Litter size
- OBSERVATIONS
- 1.5.1Clinical observations
- 1.5.2Body weight and food/water consumption of parent animals
- 1.5.3Oestrus cycle
- 1.5.4Sperm parameters
- 1.5.5Offspring
- 1.5.6Gross necropsy
- 1.5.7Organ weights
- Histopathology
- 1.5.8.1Parental Animals
- 1.5.8.2Weanlings
- DATA
- 2.1TREATMENT OF RESULTS
- 2.2EVALUATION OF RESULTS
- 2.3INTERPRETATION OF RESULTS
- REPORTING
- TEST REPORT
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- (13)Division (13)
- (14)Division (14)
- (15)Division (15)
- (16)Division (16)
- (17)Division (17)
- (18)Division (18)
- (19)Division (19)
- (20)Division (20)
- (21)Division (21)
- (22)Division (22)
- (23)Division (23)
- Annex 2H
- SKIN SENSITISATION: LOCAL LYMPH NODE ASSAY
- 1METHOD
- 1.1INTRODUCTION
- 1.2PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- Preparations
- 1.3.1.1Housing and feeding conditions
- 1.3.1.2Preparation of animals
- Test Conditions
- 1.3.2.1Experimental animals
- 1.3.2.2Reliability check
- 1.3.2.3Number of animals, dose levels and vehicle selection.
- Test procedure
- 1.3.3.1Experimental schedule
- 1.3.3.2Preparation of cell suspensions
- 1.3.3.3Determination of cell proliferation (incorporated radioactivity)
- 1.3.3.4Observations
- 1.3.4Calculation of results
- 2DATA
- REPORTING
- TEST REPORT
- REFERENCES
- 1Division 1
- 2Division 2
- 3Division 3
- 4Division 4
- 5Division 5
- 6Division 6
- 7Division 7
- 8Division 8
- 9Division 9
- 10Division 10
- 11Division 11
- 12Division 12
- 13Division 13
- 14Division 14
- NEUROTOXICITY STUDY IN RODENTS
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3PRINCIPLE OF THE TEST METHOD
- DESCRIPTION OF THE TEST METHOD
- 1.4.1Selection of animal species
- 1.4.2Housing and feeding conditions
- 1.4.3Preparation of animals
- 1.4.4Route of administration and preparation of doses
- PROCEDURES
- 1.5.1Number and sex animals
- 1.5.2Treatment and control group
- 1.5.3Reliability check
- 1.5.4Dose selection
- 1.5.5Limit test
- 1.5.6Administration of doses
- OBSERVATION
- 1.6.1Frequency of observations and tests
- 1.6.1.1Observations of general health condition and mortality/morbidity
- 1.6.1.2Detailed clinical observations
- 1.6.1.3Functional tests
- 1.6.2Body weight and food/water consumption
- 1.6.3Ophthalmology
- 1.6.4Haematology and clinical biochemistry
- 1.6.5Histopathology
- DATA
- 2.1TREATMENT OF RESULTS
- 2.2EVALUATION AND INTERPRETATION OF RESULTS
- 3REPORTING
- 4REFERENCES
- 1Division 1
- 2Division 2
- 3Division 3
- 4Division 4
- 5Division 5
- 6Division 6
- 7Division 7
- 8Division 8
- 9Division 9
- 10Division 10
- 11Division 11
- 12Division 12
- 13Division 13
- 14Division 14
- 15Division 15
- 16Division 16
- 17Division 17
- 18Division 18
- Annex 2I
- SOIL MICROORGANISMS: NITROGEN TRANSFORMATION TEST
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3REFERENCE SUBSTANCES
- 1.4PRINCIPLE OF THE TEST METHOD
- 1.5VALIDITY OF THE TEST
- DESCRIPTION OF THE TEST METHOD
- 1.6.1Apparatus
- 1.6.2Selection and number of soils
- Collection and storage of soil samples
- 1.6.3.1Collection
- 1.6.3.2Storage
- Handling and preparation of soil for the test
- 1.6.4.1Pre-incubation
- 1.6.4.2Physical-chemical characteristics
- 1.6.4.3Amendment with organic substrate
- 1.6.5Preparation of the test substance for the application to soil
- 1.6.6Test concentrations
- PERFORMANCE OF THE TEST
- Conditions of exposure
- 1.7.1.1Treatment and control
- 1.7.1.2Incubation of soil samples
- 1.7.1.3Test conditions and duration
- Sampling and analysis of soils
- 1.7.2.1Soil sampling schedule
- 1.7.2.2Analysis of soil samples
- DATA
- 2.1TREATMENT OF RESULTS
- 2.2INTERPRETATION OF RESULTS
- 3REPORTING
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- SOIL MICROORGANISMS: CARBON TRANSFORMATION TEST
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3REFERENCE SUBSTANCES
- 1.4PRINCIPLE OF THE TEST METHOD
- 1.5VALIDITY OF THE TEST
- DESCRIPTION OF THE TEST METHOD
- 1.6.1Apparatus
- 1.6.2Selection and number of soils
- Collection and storage of soil samples
- 1.6.3.1Collection
- 1.6.3.2Storage
- Handling and preparation of soil for the test
- 1.6.4.1Pre-incubation
- 1.6.4.2Physical-chemical characteristics
- 1.6.5Preparation of the test substance for the application to soil
- 1.6.6Test concentrations
- PERFORMANCE OF THE TEST
- Conditions of exposure
- 1.7.1.1Treatment and control
- 1.7.1.2Incubation of soil samples
- 1.7.1.3Test conditions and duration
- Sampling and analysis of soils
- 1.7.2.1Soil sampling schedule
- 1.7.2.2Measurement of glucose-induced respiration rates
- DATA
- 2.1TREATMENT OF RESULTS
- 2.2INTERPRETATION OF RESULTS
- REPORTING
- TEST REPORT
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- (13)Division (13)
- (14)Division (14)
- (15)Division (15)
- (16)Division (16)
- (17)Division (17)
- AEROBIC AND ANAEROBIC TRANSFORMATION IN SOIL
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3REFERENCE SUBSTANCES
- 1.4APPLICABILITY OF THE TEST
- 1.5INFORMATION ON THE TEST SUBSTANCE
- 1.6PRINCIPLE OF THE TEST METHOD
- QUALITY CRITERIA
- 1.7.1Recovery
- 1.7.2Repeatability and sensitivity of analytical method
- 1.7.3Accuracy of transformation data
- DESCRIPTION OF THE TEST METHOD
- 1.8.1Equipment and chemical reagents
- 1.8.2Test substance application
- Soils
- 1.8.3.1Soil selection
- 1.8.3.2Collection, handling, and storage of soils
- PERFORMANCE OF THE TEST
- Test conditions
- 1.9.1.1Test temperature
- 1.9.1.2Moisture content
- 1.9.1.3Aerobic incubation conditions
- 1.9.1.4Sterile aerobic conditions
- 1.9.1.5Anaerobic incubation conditions
- 1.9.1.6Paddy incubation conditions
- 1.9.1.7Test duration
- 1.9.2Performance of the test
- 1.9.3Sampling and measurement
- 1.9.4Optional tests
- DATA
- 2.1TREATMENT OF RESULTS
- 2.2EVALUATION AND INTERPRETATION OF RESULTS
- REPORTING
- TEST REPORT
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- (13)Division (13)
- (14)Division (14)
- (15)Division (15)
- (16)Division (16)
- (17)Division (17)
- (18)Division (18)
- (19)Division (19)
- (20)Division (20)
- (21)Division (21)
- (22)Division (22)
- (23)Division (23)
- (24)Division (24)
- (25)Division (25)
- (26)Division (26)
- (27)Division (27)
- (28)Division (28)
- (29)Division (29)
- (30)Division (30)
- (31)Division (31)
- (32)Division (32)
- (33)Division (33)
- (34)Division (34)
- (35)Division (35)
- (36)Division (36)
- (37)Division (37)
- ANNEX 1WATER TENSION, FIELD CAPACITY (FC) AND WATER HOLDING CAPACITY (WHC)(1)
- (1)Division (1)
- ANNEX 3
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- AEROBIC AND ANAEROBIC TRANSFORMATION IN AQUATIC SEDIMENT SYSTEMS
- 1METHOD
- 1.1INTRODUCTION
- 1.2DEFINITIONS
- 1.3REFERENCE SUBSTANCES
- 1.4INFORMATION ON THE TEST SUBSTANCE
- Division
- 1.5PRINCIPLE OF THE TEST METHOD
- 1.6APPLICABILITY OF THE TEST
- QUALITY CRITERIA
- 1.7.1Recovery
- 1.7.2Repeatability and sensitivity of analytical method
- 1.7.3Accuracy of transformation data
- DESCRIPTION OF THE METHOD
- 1.8.1Test system and apparatus
- 1.8.2Selection and number of aquatic sediments
- 1.8.2.1Sediment selection
- 1.8.2.2Characterisation of water-sediment samples
- Collection, Handling and Storage
- 1.8.3.1Collection
- 1.8.3.2Handling
- 1.8.3.3Storage
- 1.8.4Preparation of the sediment/water samples for the test
- PERFORMANCE OF THE TEST
- 1.9.1Test conditions
- 1.9.2Treatment and application of test substance
- 1.9.3Test duration and sampling
- 1.9.4Optional preliminary test
- 1.9.5Measurements and analysis
- DATA
- 2.1TREATMENT OF RESULTS
- REPORTING
- 3.1TEST REPORT
- REFERENCES
- (1)Division (1)
- (2)Division (2)
- (3)Division (3)
- (4)Division (4)
- (5)Division (5)
- (6)Division (6)
- (7)Division (7)
- (8)Division (8)
- (9)Division (9)
- (10)Division (10)
- (11)Division (11)
- (12)Division (12)
- (13)Division (13)
- (14)Division (14)
- (15)Division (15)
- (16)Division (16)
- (17)Division (17)
- (18)Division (18)
- (19)Division (19)
- (20)Division (20)
- (21)Division (21)
- (22)Division (22)
- (23)Division (23)
- (24)Division (24)
- (25)Division (25)
- (26)Division (26)
- (27)Division (27)
- (28)Division (28)
- (29)Division (29)
- (30)Division (30)
- (31)Division (31)
- (32)Division (32)
- (33)Division (33)
- (34)Division (34)
- (35)Division (35)
- (36)Division (36)
- (37)Division (37)
- GUIDANCE ON THE AEROBIC AND THE ANAEROBIC TEST SYSTEMS
- Aerobic test system
- Anaerobic test system
- ANNEX 2EXAMPLE OF A GAS FLOW-THROUGH APPARATUS