Division 52 Testing should be carried out according to Great Britain guidelines where these are available and applicable. Where appropriate, other methods from the list below can be used. If relevant acceptable field data exist, these can be used.F1
United Kingdom
ISO, CEN or other international standard method
national standard method
industry standard method (if accepted by the F2competent authority)
individual producer standard method (if accepted by the competent authority)
data from the actual development of the biocidal product (if accepted by the competent authority).
Annotations
Textual amendments
- F1
Words in Annex 6 para. 52 substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 143(12) (as amended by S.I. 2020/1567, reg. 1(2), Sch. 2 para. 39(a)); 2020 c. 1, Sch. 5 para. 1(1)
- F2
Words in Annex 6 para. 52 substituted (31.12.2020) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/720), reg. 1(2), Sch. 2 para. 143(11); 2020 c. 1, Sch. 5 para. 1(1)