Paragraph 35 I1
United Kingdom
In Article 38—
in the heading, for “harmonised” substitute “ mandatory ” and for “Part 3 of Annex VI” substitute “ the F1GB mandatory classification and labelling list ”;
before paragraph 1, insert a new paragraph—
“A1Any opinion of the Agency referred to in Article 37 must specify the reasons for the opinion.”;
in paragraph 1, for “referred to in Article 37(4) and any decision according to Article 37(5)” substitute “ of the Agency referred to in Article 37A ”;
for paragraph 2, substitute—
“2When making publicly available an opinion or a decision as referred to in Article 37 or Article 37A, the Agency must not publish any information in relation to which paragraph 3 applies.”;
after paragraph 2, insert—
“3This paragraph applies to information which has been made available to the Agency in relation to which a person has submitted a justification, accepted by the Agency as valid, as to why publication of the information is potentially harmful to the commercial interests of that person or any other person.”
Annotations
Textual amendments
- F1
Word in Sch. 2 para. 35 substituted (31.12.2020 immediately before IP completion day) by The Chemicals (Health and Safety) and Genetically Modified Organisms (Contained Use) (Amendment etc.) (EU Exit) Regulations 2020 (S.I. 2020/1567), reg. 1(2), Sch. 2 para. 9(a)
Commencement
- I1
Sch. 2 para. 35 in force at 31.12.2020 on IP completion day (in accordance with 2020 c. 1, Sch. 5 para. 1(1)), see reg. 1(2)