This standard defines the requirements for a training programme to train risk assessors to be competent to assess the health risks posed by chemical substances.

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This European Standard specifies the minimum requirements for a course programme to train risk assessors to be competent to assess the health risks posed by chemicals.
This European Standard does not comprehensively cover requirements for qualifications for workplace risk assessment according to Directive 98/24/EC.
Training of risk assessors consists of both course programs and on-the-job, practical experience. Only the course-based programme is covered in the current standard.
This European Standard sets out the requirements, which may be delivered as a complete course programme or as a series of individual courses.

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CEN/TR 16721 gives an overview of methods which can be used for the determination of the bio-based content of solid, liquid and gaseous products. It describes more specifically: a) a method using the radiocarbon analysis and elemental analysis: this method is based on a statement and a verification of the composition of the products; b) methods based on measurement of stable isotopic ratio; and c) a method based on the material balance. This Technical Report gives guidance on the applicability of the different methods. This Technical Report also gives recommendations for the further development of European Standards for the determination of the bio-based content.

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ISO 10808:2010 specifies requirements for, and gives guidance on, the characterization of airborne nanoparticles in inhalation exposure chambers for the purpose of inhalation toxicity studies in terms of particle mass, size distribution, number concentration and composition.

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ISO 10801:2010 gives requirements and recommendations for generating metal nanoparticles as aerosols suitable for inhalation toxicity testing by the evaporation/condensation method. Its application is limited to metals such as gold and silver which have been proven to generate nanoparticles suitable for inhalation toxicity testing using the technique specified.

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ISO 29701:2010 describes the application of a test using Limulus amebocyte lysate (LAL) reagent for the evaluation of nanomaterials intended for cell-based in vitro biological test systems. The test is suitable for use with nanomaterial samples dispersed in aqueous media, e.g. water, serum or reaction medium, and to such media incubated with nanomaterials for an appropriate duration at 37 °C.
ISO 29701:2010 is restricted to test samples for in vitro systems, but the methods can also be adapted to nanomaterials to be administered to animals by parenteral routes.

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ISO 11014:2009 defines sections, content, and general format of the safety data sheet (SDS) for chemical products. ISO 11014:2009 does not define a fixed format, nor does it include a blank SDS.

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Presents information for the compilation and completion of a safety data sheet. Defines specifically the general layout of the SDS, the 16 standard headings, the numbering and the sequence of these 16 standard headings, the items necessary to fill in an SDS and the conditions of their applicability or utilization.

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