This regulation amends (EU) No 582/2011 with respect to emissions from heavy-duty vehicles as regards the provisions on testing by means of portable emission measurement systems (PEMS) and the procedure for the testing of the durability of replacement pollution control devices. Comes into force 10th October.
The Order amends the Capital Allowances (Environmentally Beneficial Plant and Machinery) Order 2003 (SI 2003/2076).
Article 3 amends the definitions of the “Water Technology Criteria List” and the “Water Technology Product List” to refer to the new lists, which are available at https://www.gov.uk/government/publications/water-efficient-enhanced-capital-allowances.
Article 4 revokes the Capital Allowances (Environmentally Beneficial Plant and Machinery) (Amendment) Order 2016 (S.I. 2016/926) which contained an error at article 3(a).
EU regulation amending Annex VII to Regulation (EC) No 1907/2006 on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) as regards skin sensitisation.
8.3. Skin sensitisation
a conclusion whether the substance is a skin sensitiser and whether it can be presumed to have the potential to produce significant sensitisation in humans (Cat. 1A), and
risk assessment, where required.
The study(ies) under point 8.3.1 and 8.3.2 do not need to be conducted if:
the substance is classified as skin corrosion (Category 1), or
the substance is a strong acid (pH ≤ 2,0) or base (pH ≥ 11,5), or
the substance is spontaneously flammable in air or in contact with water or moisture at room temperature.
8.3.1. Skin sensitisation, in vitro/in chemico
Information from in vitro/in chemico test method(s) recognised according to Article 13(3), addressing each of the following key events of skin sensitisation:
molecular interaction with skin proteins;
inflammatory response in keratinocytes;
activation of dendritic cells.
The(se) test(s) do not need to be conducted if
an in vivo study according to point 8.3.2 is available, or
the available in vitro/in chemico test methods are not applicable for the substance or are not adequate for classification and risk assessment according to point 8.3.
If information from test method(s) addressing one or two of the key events in column 1 already allows classification and risk assessment according to point 8.3, studies addressing the other key event(s) need not be conducted.
8.3.2. Skin sensitisation, in vivo
An in vivo study shall be conducted only if in vitro/in chemico test methods described under point 8.3.1 are not applicable, or the results obtained from those studies are not adequate for classification and risk assessment according to point 8.3.
The murine local lymph node assay (LLNA) is the first-choice method for in vivo testing. Only in exceptional circumstances should another test be used. Justification for the use of another in vivo test shall be provided.
In vivo skin sensitisation studies that were carried out or initiated before 11 October 2016, and that meet the requirements set out in Article 13(3), first subparagraph, and Article 13(4) shall be considered appropriate to address this standard information requirement