http://www.legislation.gov.uk/eur/2014/1062/article/5Commission Delegated Regulation (EU) No 1062/2014 of 4 August 2014 on the work programme for the systematic examination of all existing active substances contained in biocidal products referred to in Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)Commission Delegated Regulation (EU) No 1062/2014Commission Delegated Regulation (EU) No 1062/2014 of 4 August 2014 on the work programme for the systematic examination of all existing active substances contained in biocidal products referred to in Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)King's Printer of Acts of Parliamenthttps://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02014R1062-20190330texttext/xmlen2025-04-23Expert Participation2025-02-27 CHAPTER 2 <Strong>PROCESS FOR EVALUATION OF DOSSIERS</Strong> Validation of applications for approval or inclusion in <Substitution ChangeId="key-3303317b109998f8297a5a90c2dc05fc-1732902523000" CommentaryRef="key-3303317b109998f8297a5a90c2dc05fc">category B</Substitution> of <Substitution ChangeId="key-b0e494e736f15df2368949481d59ca22-1732813061000" CommentaryRef="key-b0e494e736f15df2368949481d59ca22">the Simplified Active Substance List</Substitution>Article 51Where an application for approval or inclusion in category B of the Simplified Active Substance List containing the data required in accordance with Article 6(1) and (2) of Regulation (EU) No 528/2012 has been accepted by the competent authority and the appropriate fee has been paid pursuant to Article 4 the competent authority shall validate the application within 30 days of that payment.2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3In the cases referred to in paragraph 1, the ... competent authority shall not make an assessment of the quality or the adequacy of the data or justifications submitted.4Where the ... competent authority considers that the application is incomplete, it shall inform the participant as to what additional information is required for the validation of the application and shall set a reasonable time limit for the submission of that information. That time limit shall not normally exceed 90 days.The ... competent authority shall, within 30 days of receipt of the additional information, validate the application if it determines that the additional information submitted is sufficient to comply with the requirement laid down in paragraph 1.The ... competent authority shall reject the application if the participant fails to submit the requested information within the deadline and shall inform the participant ... accordingly. In such cases, part of the appropriate fees paid shall be reimbursed.On validating an application, the ... competent authority shall without delay inform the participant, ... indicating the date of the validation.Words in Art. 5 heading 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. 217(2); 2020 c. 1, Sch. 5 para. 1(1)Art. 5(1) 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. 217(3); 2020 c. 1, Sch. 5 para. 1(1)Art. 5(2) omitted (31.12.2020) by virtue of 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. 217(4); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 5(3) 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. 217(5)(i); 2020 c. 1, Sch. 5 para. 1(1)Word in Art. 5(3) omitted (31.12.2020) by virtue of 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. 217(5)(ii); 2020 c. 1, Sch. 5 para. 1(1)Word in Art. 5(4) 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. 217(6)(b); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 5(4) omitted (31.12.2020) by virtue of 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. 217(6)(c)(i); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 5(4) 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. 217(6)(c)(ii); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 5(4) omitted (31.12.2020) by virtue of 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. 217(6)(d); 2020 c. 1, Sch. 5 para. 1(1)Word in Art. 5(4) omitted (31.12.2020) by virtue of 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. 217(6)(a); 2020 c. 1, Sch. 5 para. 1(1)Words in Art. 5 heading substituted (1.11.2022) by The Chemicals (Health and Safety) Trade and Miscellaneous Amendments Regulations 2022 (S.I. 2022/1037), regs. 1(2), 10(2)Words in Art. 5(1) substituted (1.11.2022) by The Chemicals (Health and Safety) Trade and Miscellaneous Amendments Regulations 2022 (S.I. 2022/1037), regs. 1(2), 10(3)